rs55737008
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Rare Variant(gnomAD Genomes)Learn more about rare variants(opens in new window)
Locations
| Assembly | Sequence | Position | Alleles | Source |
|---|---|---|---|---|
| GRCh38 | NC_000012.12(opens in new window) | 21239113 |
| Pharmacogene Variation Consortium |
| GRCh38 | NC_000012.12(opens in new window) | 21239113 |
| dbSnp |
| GRCh37 | NC_000012.11(opens in new window) | 21392047 |
| dbSnp |
| NG_011745.1(opens in new window) | 112920 |
| dbSnp | |
| NP_006437.3(opens in new window) | 667 |
| dbSnp | |
| GRCh38 | NC_000012.12(opens in new window) | 21239113 |
| PharmGKB Haplotype |
Variant Frequencies
This variant is considered rare based on global allele frequencies based on data from gnomAD Genomes. more info
Identifiers
PharmGKB ID
Aliases
- NC_000012.11:g.21392047A>G
- NC_000012.12:g.21239113A>G
- NG_011745.1:g.112920A>G
- NM_006446.4:c.2000A>G
- NP_006437.3:p.Glu667Gly
History
No history available.