HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133255622G= , CM000671.2:g.133255622G= | GRCh38 |
NC_000009.11:g.136131009G= , CM000671.1:g.136131009G= | GRCh37 |
NC_000009.10:g.135120830G= | NCBI36 |
NG_006669.1:g.22046C= | |
NG_006669.2:g.24594C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000453660.4:n.1138C= | ||
ENST00000647353.1:n.54-4470C= | ||
ENST00000679909.1:c.28+19540C= | ENSP00000506089.1:n.28+19540C= | |
ENST00000453660.3:n.1120C= | ||
ENST00000538324.2:c.1102C= | ENSP00000483018.1:p.Pro368= | |
ENST00000611156.4:c.*44C= | ENSP00000483265.1:n.*44C= | |
NM_020469.2:c.*44C= | NP_065202.2:n.*44C= | |
NM_020469.3:c.*44C= | NP_065202.2:n.*44C= |