HGVS | Genome Assembly |
---|---|
NC_000002.12:g.38074967C>T , CM000664.2:g.38074967C>T | GRCh38 |
NC_000002.11:g.38302110C>T , CM000664.1:g.38302110C>T | GRCh37 |
NC_000002.10:g.38155614C>T | NCBI36 |
NG_008386.2:g.6135G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000490576.2:c.422G>A | ENSP00000478839.2:p.Trp141Ter | |
ENST00000610745.5:c.422G>A MANE Select | ENSP00000478561.1:p.Trp141Ter | |
ENST00000490576.1:c.422G>A | ENSP00000478839.1:p.Trp141Ter | |
ENST00000494864.1:c.-70-3657G>A | ENSP00000479876.1:n.-70-3657G>A | |
ENST00000610745.4:c.422G>A | ENSP00000478561.1:p.Trp141Ter | |
ENST00000613082.1:n.376-559G>A | ||
ENST00000614273.1:c.422G>A | ENSP00000483678.1:p.Trp141Ter | |
NM_000104.3:c.422G>A | NP_000095.2:p.Trp141Ter | |
NM_000104.4:c.422G>A MANE Select | NP_000095.2:p.Trp141Ter |