Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.125241700G>A , CM000671.2:g.125241700G>A | GRCh38 |
| NC_000009.11:g.128003979G>A , CM000671.1:g.128003979G>A | GRCh37 |
| NC_000009.10:g.127043800G>A | NCBI36 |
| NG_027761.1:g.4688C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XM_011518501.1:c.-705G>A (GAPVD1) | XP_011516803.1:n.-705G>A |
| XM_011518503.1:c.-1011G>A (GAPVD1) | XP_011516805.1:n.-1011G>A |
| XM_011518504.1:c.-656G>A (GAPVD1) | XP_011516806.1:n.-656G>A |
| XR_001746927.1:n.38G>A (HSPA5-DT) |