Linked Data
MyVariant Identifiers:
chr9:g.128004013C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.125241734C>G , CM000671.2:g.125241734C>G | GRCh38 |
| NC_000009.11:g.128004013C>G , CM000671.1:g.128004013C>G | GRCh37 |
| NC_000009.10:g.127043834C>G | NCBI36 |
| NG_027761.1:g.4654G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011518501.1:c.-671C>G (GAPVD1) | XP_011516803.1:n.-671C>G | |
| XM_011518503.1:c.-977C>G (GAPVD1) | XP_011516805.1:n.-977C>G | |
| XM_011518504.1:c.-622C>G (GAPVD1) | XP_011516806.1:n.-622C>G | |
| XR_001746927.1:n.72C>G (HSPA5-DT) |