HGVS | Genome Assembly |
---|---|
NC_000003.12:g.129529094G>T , CM000665.2:g.129529094G>T | GRCh38 |
NC_000003.11:g.129247937G>T , CM000665.1:g.129247937G>T | GRCh37 |
NC_000003.10:g.130730627G>T | NCBI36 |
NG_009115.1:g.5456G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000296271.4:c.361G>T MANE Select | ENSP00000296271.3:p.Gly121Cys | |
ENST00000296271.3:c.361G>T | ENSP00000296271.3:p.Gly121Cys | |
NM_000539.3:c.361G>T MANE Select | NP_000530.1:p.Gly121Cys |