HGVS | Genome Assembly |
---|---|
NC_000010.11:g.46046596A>T , CM000672.2:g.46046596A>T | GRCh38 |
NC_000010.10:g.51549226T>A , CM000672.1:g.51549226T>A | GRCh37 |
NC_000010.9:g.51219232T>A | NCBI36 |
NG_011551.1:g.4674T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000663171.1:c.-142-217T>A | ENSP00000499419.1:n.-142-217T>A |