HGVS | Genome Assembly |
---|---|
NC_000003.12:g.190404816T>A , CM000665.2:g.190404816T>A | GRCh38 |
NC_000003.11:g.190122605T>A , CM000665.1:g.190122605T>A | GRCh37 |
NC_000003.10:g.191605299T>A | NCBI36 |
NG_008149.1:g.21765T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264734.3:c.272T>A MANE Select | ENSP00000264734.3:p.Phe91Tyr | |
ENST00000456423.2:c.115-5087T>A | ENSP00000414136.2:n.115-5087T>A | |
ENST00000264734.2:c.482T>A | ENSP00000264734.2:p.Phe161Tyr | |
ENST00000456423.1:c.325-5087T>A | ENSP00000414136.1:n.325-5087T>A | |
ENST00000468220.1:n.464T>A | ||
NM_006580.3:c.482T>A | NP_006571.1:p.Phe161Tyr | |
NM_001378492.1:c.272T>A | NP_001365421.1:p.Phe91Tyr | |
NM_001378493.1:c.272T>A | NP_001365422.1:p.Phe91Tyr | |
NM_006580.4:c.272T>A MANE Select | NP_006571.2:p.Phe91Tyr |