HGVS | Genome Assembly |
---|---|
NC_000004.12:g.67932024T>A , CM000666.2:g.67932024T>A | GRCh38 |
NC_000004.11:g.68797742T>A , CM000666.1:g.68797742T>A | GRCh37 |
NC_000004.10:g.68480337T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000508048.6:c.289A>T MANE Select | ENSP00000426911.2:p.Asn97Tyr | |
ENST00000334830.11:c.298A>T | ENSP00000334611.7:p.Asn100Tyr | |
ENST00000396188.3:c.289A>T | ENSP00000379491.3:p.Asn97Tyr | |
ENST00000508048.5:c.289A>T | ENSP00000426911.2:p.Asn97Tyr | |
ENST00000513536.5:c.229A>T | ENSP00000427621.1:p.Asn77Tyr | |
NM_001114387.1:c.289A>T | NP_001107859.1:p.Asn97Tyr | |
NM_182606.3:c.298A>T | NP_872412.3:p.Asn100Tyr | |
NM_001114387.2:c.289A>T MANE Select | NP_001107859.1:p.Asn97Tyr | |
NM_182606.4:c.298A>T | NP_872412.3:p.Asn100Tyr |