Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.125241745T>A , CM000671.2:g.125241745T>A | GRCh38 |
| NC_000009.11:g.128004024T>A , CM000671.1:g.128004024T>A | GRCh37 |
| NC_000009.10:g.127043845T>A | NCBI36 |
| NG_027761.1:g.4643A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011518501.1:c.-660T>A (GAPVD1) | XP_011516803.1:n.-660T>A | |
| XM_011518503.1:c.-966T>A (GAPVD1) | XP_011516805.1:n.-966T>A | |
| XM_011518504.1:c.-611T>A (GAPVD1) | XP_011516806.1:n.-611T>A | |
| XR_001746927.1:n.83T>A (HSPA5-DT) |