HGVS | Genome Assembly |
---|---|
NC_000010.11:g.46046349G>A , CM000672.2:g.46046349G>A | GRCh38 |
NC_000010.10:g.51549473C>T , CM000672.1:g.51549473C>T | GRCh37 |
NC_000010.9:g.51219479C>T | NCBI36 |
NG_011551.1:g.4921C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000663171.1:c.-112C>T | ENSP00000499419.1:n.-112C>T |