HGVS | Genome Assembly |
---|---|
NC_000019.10:g.48419645T>A , CM000681.2:g.48419645T>A | GRCh38 |
NC_000019.9:g.48922902T>A , CM000681.1:g.48922902T>A | GRCh37 |
NC_000019.8:g.53614714T>A | NCBI36 |
NG_052829.1:g.29771T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263269.4:c.1922T>A MANE Select | ENSP00000263269.2:p.Phe641Tyr | |
ENST00000263269.3:c.1922T>A | ENSP00000263269.2:p.Phe641Tyr | |
NM_000836.2:c.1922T>A | NP_000827.2:p.Phe641Tyr | |
XM_011526872.1:c.1922T>A | XP_011525174.1:p.Phe641Tyr | |
NM_000836.4:c.1922T>A MANE Select | NP_000827.2:p.Phe641Tyr |