HGVS | Genome Assembly |
---|---|
NC_000009.12:g.21140510A>T , CM000671.2:g.21140510A>T | GRCh38 |
NC_000009.11:g.21140509A>T , CM000671.1:g.21140509A>T | GRCh37 |
NC_000009.10:g.21130509A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000380229.3:c.*473T>A | ENSP00000369578.2:n.*473T>A |