HGVS | Genome Assembly |
---|---|
NC_000019.10:g.1399847G>A , CM000681.2:g.1399847G>A | GRCh38 |
NC_000019.9:g.1399846G>A , CM000681.1:g.1399846G>A | GRCh37 |
NC_000019.8:g.1350846G>A | NCBI36 |
NG_009785.1:g.6707C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000252288.8:c.273C>T MANE Select | ENSP00000252288.1:p.Cys91= | |
ENST00000447102.8:c.273C>T | ENSP00000403536.2:p.Cys91= | |
ENST00000640762.1:c.204C>T | ENSP00000492031.1:p.Cys68= | |
ENST00000252288.6:c.273C>T | ENSP00000252288.1:p.Cys91= | |
ENST00000447102.7:c.273C>T | ENSP00000403536.2:p.Cys91= | |
NM_000156.5:c.273C>T | NP_000147.1:p.Cys91= | |
NM_138924.2:c.273C>T | NP_620279.1:p.Cys91= | |
NM_000156.6:c.273C>T MANE Select | NP_000147.1:p.Cys91= | |
NM_138924.3:c.273C>T | NP_620279.1:p.Cys91= |