HGVS | Genome Assembly |
---|---|
NC_000010.11:g.46046563T>A , CM000672.2:g.46046563T>A | GRCh38 |
NC_000010.10:g.51549259A>T , CM000672.1:g.51549259A>T | GRCh37 |
NC_000010.9:g.51219265A>T | NCBI36 |
NG_011551.1:g.4707A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000663171.1:c.-142-184A>T | ENSP00000499419.1:n.-142-184A>T |