HGVS | Genome Assembly |
---|---|
NC_000002.12:g.227805859G>T , CM000664.2:g.227805859G>T | GRCh38 |
NC_000002.11:g.228670575G>T , CM000664.1:g.228670575G>T | GRCh37 |
NC_000002.10:g.228378819G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000646475.1:c.-201G>T | ENSP00000496658.1:n.-201G>T |