HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133255634C= , CM000671.2:g.133255634C= | GRCh38 |
NC_000009.11:g.136131021C= , CM000671.1:g.136131021C= | GRCh37 |
NC_000009.10:g.135120842C= | NCBI36 |
NG_006669.1:g.22034G= | |
NG_006669.2:g.24582G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000453660.4:n.1126G= | ||
ENST00000647353.1:n.54-4482G= | ||
ENST00000679909.1:c.28+19528G= | ENSP00000506089.1:n.28+19528G= | |
ENST00000453660.3:n.1108G= | ||
ENST00000538324.2:c.1090G= | ENSP00000483018.1:p.Ala364= | |
ENST00000611156.4:c.*32G= | ENSP00000483265.1:n.*32G= | |
NM_020469.2:c.*32G= | NP_065202.2:n.*32G= | |
NM_020469.3:c.*32G= | NP_065202.2:n.*32G= |