HGVS | Genome Assembly |
---|---|
NC_000019.10:g.45804328A>T , CM000681.2:g.45804328A>T | GRCh38 |
NC_000019.9:g.46307586A>T , CM000681.1:g.46307586A>T | GRCh37 |
NC_000019.8:g.50999426A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000221538.8:c.1577T>A MANE Select | ENSP00000221538.2:p.Phe526Tyr | |
ENST00000221538.7:c.1577T>A | ENSP00000221538.2:p.Phe526Tyr | |
ENST00000597055.1:c.1577T>A | ENSP00000472630.1:p.Phe526Tyr | |
ENST00000600188.5:c.785T>A | ENSP00000471559.1:p.Phe262Tyr | |
NM_030785.3:c.1577T>A | NP_110412.1:p.Phe526Tyr | |
XM_011527351.1:c.1577T>A | XP_011525653.1:p.Phe526Tyr | |
XM_011527351.2:c.1577T>A | XP_011525653.1:p.Phe526Tyr | |
NM_030785.4:c.1577T>A MANE Select | NP_110412.1:p.Phe526Tyr |