HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133255939G>A , CM000671.2:g.133255939G>A | GRCh38 |
NC_000009.11:g.136131326G>A , CM000671.1:g.136131326G>A | GRCh37 |
NC_000009.10:g.135121147G>A | NCBI36 |
NG_006669.1:g.21729C>T | |
NG_006669.2:g.24277C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000453660.4:n.821C>T | ||
ENST00000647353.1:n.54-4787C>T | ||
ENST00000679909.1:c.28+19223C>T | ENSP00000506089.1:n.28+19223C>T | |
ENST00000453660.3:n.803C>T | ||
ENST00000538324.2:c.789C>T | ENSP00000483018.1:p.Tyr263= | |
ENST00000611156.4:c.789C>T | ENSP00000483265.1:p.Tyr263= | |
NM_020469.2:c.792C>T | NP_065202.2:p.Tyr264= | |
NM_020469.3:c.792C>T | NP_065202.2:p.Tyr264= |