HGVS | Genome Assembly |
---|---|
NC_000011.10:g.69648095T>A , CM000673.2:g.69648095T>A | GRCh38 |
NC_000011.9:g.69462863T>A , CM000673.1:g.69462863T>A | GRCh37 |
NC_000011.8:g.69172044T>A | NCBI36 |
NG_007375.1:g.11991T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000227507.3:c.676T>A MANE Select | ENSP00000227507.2:p.Tyr226Asn | |
ENST00000227507.2:c.676T>A | ENSP00000227507.2:p.Tyr226Asn | |
ENST00000536559.1:c.*96T>A | ENSP00000438482.1:n.*96T>A | |
ENST00000542367.1:n.139T>A | ||
ENST00000545484.1:n.382T>A | ||
NM_053056.2:c.676T>A | NP_444284.1:p.Tyr226Asn | |
XM_006718653.2:c.700T>A | XP_006718716.1:p.Tyr234Asn | |
NM_053056.3:c.676T>A MANE Select | NP_444284.1:p.Tyr226Asn |