HGVS | Genome Assembly |
---|---|
NC_000017.11:g.74920009A>T , CM000679.2:g.74920009A>T | GRCh38 |
NC_000017.10:g.72916104A>T , CM000679.1:g.72916104A>T | GRCh37 |
NC_000017.9:g.70427699A>T | NCBI36 |
NG_007882.1:g.8248T>A | |
NG_033062.1:g.735A>T | |
NG_007882.2:g.8255T>A | |
NG_033062.2:g.735A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000614341.5:c.827T>A MANE Select | ENSP00000480279.1:p.Phe276Tyr | |
ENST00000579243.1:c.*426T>A | ENSP00000462568.1:n.*426T>A | |
ENST00000614341.4:c.827T>A | ENSP00000480279.1:p.Phe276Tyr | |
NM_001282489.2:c.518T>A | NP_001269418.1:p.Phe173Tyr | |
NM_173477.4:c.827T>A | NP_775748.2:p.Phe276Tyr | |
XM_011524296.1:c.518T>A | XP_011522598.1:p.Phe173Tyr | |
XM_011524296.2:c.518T>A | XP_011522598.1:p.Phe173Tyr | |
NM_173477.5:c.827T>A MANE Select | NP_775748.2:p.Phe276Tyr | |
NM_001282489.3:c.518T>A | NP_001269418.1:p.Phe173Tyr |