Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.125241728T>C , CM000671.2:g.125241728T>C | GRCh38 |
| NC_000009.11:g.128004007T>C , CM000671.1:g.128004007T>C | GRCh37 |
| NC_000009.10:g.127043828T>C | NCBI36 |
| NG_027761.1:g.4660A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011518501.1:c.-677T>C (GAPVD1) | XP_011516803.1:n.-677T>C | |
| XM_011518503.1:c.-983T>C (GAPVD1) | XP_011516805.1:n.-983T>C | |
| XM_011518504.1:c.-628T>C (GAPVD1) | XP_011516806.1:n.-628T>C | |
| XR_001746927.1:n.66T>C (HSPA5-DT) |