HGVS | Genome Assembly |
---|---|
NC_000016.10:g.89179514G>A , CM000678.2:g.89179514G>A | GRCh38 |
NC_000016.9:g.89245922G>A , CM000678.1:g.89245922G>A | GRCh37 |
NC_000016.8:g.87773423G>A | NCBI36 |
NG_012055.1:g.12760G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000289746.3:c.141G>A MANE Select | ENSP00000289746.2:p.Trp47Ter | |
ENST00000289746.2:c.141G>A | ENSP00000289746.2:p.Trp47Ter | |
ENST00000521087.5:n.206G>A | ||
ENST00000524089.1:n.206G>A | ||
NM_004933.2:c.141G>A | NP_004924.1:p.Trp47Ter | |
XM_011522806.1:c.141G>A | XP_011521108.1:p.Trp47Ter | |
NM_004933.3:c.141G>A MANE Select | NP_004924.1:p.Trp47Ter |