HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133255664G= , CM000671.2:g.133255664G= | GRCh38 |
NC_000009.11:g.136131051G= , CM000671.1:g.136131051G= | GRCh37 |
NC_000009.10:g.135120872G= | NCBI36 |
NG_006669.1:g.22004C= | |
NG_006669.2:g.24552C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000453660.4:n.1096C= | ||
ENST00000647353.1:n.54-4512C= | ||
ENST00000679909.1:c.28+19498C= | ENSP00000506089.1:n.28+19498C= | |
ENST00000453660.3:n.1078C= | ||
ENST00000538324.2:c.1060C= | ENSP00000483018.1:p.Arg354= | |
ENST00000611156.4:c.*2C= | ENSP00000483265.1:n.*2C= | |
NM_020469.2:c.*2C= | NP_065202.2:n.*2C= | |
NM_020469.3:c.*2C= | NP_065202.2:n.*2C= |