HGVS | Genome Assembly |
---|---|
NC_000004.12:g.67932046A>T , CM000666.2:g.67932046A>T | GRCh38 |
NC_000004.11:g.68797764A>T , CM000666.1:g.68797764A>T | GRCh37 |
NC_000004.10:g.68480359A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000508048.6:c.267T>A MANE Select | ENSP00000426911.2:p.Phe89Leu | |
ENST00000334830.11:c.276T>A | ENSP00000334611.7:p.Phe92Leu | |
ENST00000396188.3:c.267T>A | ENSP00000379491.3:p.Phe89Leu | |
ENST00000508048.5:c.267T>A | ENSP00000426911.2:p.Phe89Leu | |
ENST00000513536.5:c.207T>A | ENSP00000427621.1:p.Phe69Leu | |
NM_001114387.1:c.267T>A | NP_001107859.1:p.Phe89Leu | |
NM_182606.3:c.276T>A | NP_872412.3:p.Phe92Leu | |
NM_001114387.2:c.267T>A MANE Select | NP_001107859.1:p.Phe89Leu | |
NM_182606.4:c.276T>A | NP_872412.3:p.Phe92Leu |