HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133255912C>A , CM000671.2:g.133255912C>A | GRCh38 |
NC_000009.11:g.136131299C>A , CM000671.1:g.136131299C>A | GRCh37 |
NC_000009.10:g.135121120C>A | NCBI36 |
NG_006669.1:g.21756G>T | |
NG_006669.2:g.24304G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000453660.4:n.848G>T | ||
ENST00000647353.1:n.54-4760G>T | ||
ENST00000679909.1:c.28+19250G>T | ENSP00000506089.1:n.28+19250G>T | |
ENST00000453660.3:n.830G>T | ||
ENST00000538324.2:c.816G>T | ENSP00000483018.1:p.Ser272= | |
ENST00000611156.4:c.816G>T | ENSP00000483265.1:p.Ser272= | |
NM_020469.2:c.819G>T | NP_065202.2:p.Ser273= | |
NM_020469.3:c.819G>T | NP_065202.2:p.Ser273= |