Linked Data
MyVariant Identifiers:
chr9:g.128004069G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.125241790G>C , CM000671.2:g.125241790G>C | GRCh38 |
| NC_000009.11:g.128004069G>C , CM000671.1:g.128004069G>C | GRCh37 |
| NC_000009.10:g.127043890G>C | NCBI36 |
| NG_027761.1:g.4598C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011518501.1:c.-615G>C (GAPVD1) | XP_011516803.1:n.-615G>C | |
| XM_011518503.1:c.-921G>C (GAPVD1) | XP_011516805.1:n.-921G>C | |
| XM_011518504.1:c.-566G>C (GAPVD1) | XP_011516806.1:n.-566G>C | |
| XR_001746927.1:n.128G>C (HSPA5-DT) |