HGVS | Genome Assembly |
---|---|
NC_000006.12:g.121447009T>A , CM000668.2:g.121447009T>A | GRCh38 |
NC_000006.11:g.121768155T>A , CM000668.1:g.121768155T>A | GRCh37 |
NC_000006.10:g.121809854T>A | NCBI36 |
NG_008308.1:g.16411T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000282561.4:c.162T>A MANE Select | ENSP00000282561.3:p.Cys54Ter | |
ENST00000647564.1:c.162T>A | ENSP00000497565.1:p.Cys54Ter | |
ENST00000649003.1:c.162T>A | ENSP00000497283.1:p.Cys54Ter | |
ENST00000650427.1:c.162T>A | ENSP00000497367.1:p.Cys54Ter | |
ENST00000282561.3:c.162T>A | ENSP00000282561.3:p.Cys54Ter | |
NM_000165.4:c.162T>A | NP_000156.1:p.Cys54Ter | |
NM_000165.5:c.162T>A MANE Select | NP_000156.1:p.Cys54Ter |