HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6710839T>A , CM000681.2:g.6710839T>A | GRCh38 |
NC_000019.9:g.6710850T>A , CM000681.1:g.6710850T>A | GRCh37 |
NC_000019.8:g.6661850T>A | NCBI36 |
NG_009557.1:g.14813A>T , LRG_27:g.14813A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000695652.1:c.1363A>T | ENSP00000512083.1:p.Asn455Tyr | |
ENST00000695654.1:c.610A>T | ENSP00000512085.1:p.Asn204Tyr | |
ENST00000695655.1:c.391A>T | ENSP00000512086.1:p.Asn131Tyr | |
ENST00000695692.1:n.850A>T | ||
ENST00000245907.11:c.1486A>T MANE Select | ENSP00000245907.4:p.Asn496Tyr | |
ENST00000245907.10:c.1486A>T | ENSP00000245907.4:p.Asn496Tyr | |
ENST00000600763.1:n.119A>T | ||
NM_000064.3:c.1486A>T | NP_000055.2:p.Asn496Tyr | |
NM_000064.4:c.1486A>T MANE Select | NP_000055.2:p.Asn496Tyr |