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