HGVS | Genome Assembly |
---|---|
NC_000009.12:g.125241734C>T , CM000671.2:g.125241734C>T | GRCh38 |
NC_000009.11:g.128004013C>T , CM000671.1:g.128004013C>T | GRCh37 |
NC_000009.10:g.127043834C>T | NCBI36 |
NG_027761.1:g.4654G>A |
HGVS | Amino-acid Change | |
---|---|---|
XM_011518501.1:c.-671C>T (GAPVD1) | XP_011516803.1:n.-671C>T | |
XM_011518503.1:c.-977C>T (GAPVD1) | XP_011516805.1:n.-977C>T | |
XM_011518504.1:c.-622C>T (GAPVD1) | XP_011516806.1:n.-622C>T | |
XR_001746927.1:n.72C>T (HSPA5-DT) |