HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48410995G>A , CM000677.2:g.48410995G>A | GRCh38 |
NC_000015.9:g.48703192G>A , CM000677.1:g.48703192G>A | GRCh37 |
NC_000015.8:g.46490484G>A | NCBI36 |
NG_008805.2:g.239794C>T , LRG_778:g.239794C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559133.6:c.*1419C>T | ENSP00000453958.2:n.*1419C>T | |
ENST00000682158.1:n.1992C>T | ||
ENST00000682170.1:n.2792C>T | ||
ENST00000682767.1:n.1908C>T | ||
ENST00000316623.10:c.8611C>T MANE Select | ENSP00000325527.5:p.His2871Tyr | |
ENST00000316623.9:c.8611C>T | ENSP00000325527.5:p.His2871Tyr | |
ENST00000559133.5:c.3980C>T | ||
NM_000138.4:c.8611C>T , LRG_778t1:c.8611C>T | NP_000129.3:p.His2871Tyr | |
NM_000138.5:c.8611C>T MANE Select | NP_000129.3:p.His2871Tyr |