Canonical Allele Identifier: CA2241201237
Gene: CYBA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88646137A= , CM000678.2:g.88646137A= GRCh38
NC_000016.9:g.88712545A= , CM000678.1:g.88712545A= GRCh37
NC_000016.8:g.87240046A= NCBI36
NG_007291.1:g.9913T= , LRG_52:g.9913T=

Transcript Alleles

HGVS Amino-acid change
ENST00000565588.6:c.348T= ENSP00000455537.2:p.Ile116=
ENST00000696156.1:c.264T= ENSP00000512446.1:p.Ile88=
ENST00000696157.1:c.348T= ENSP00000512447.1:p.Ile116=
ENST00000696158.1:c.348T= ENSP00000512448.1:p.Ile116=
ENST00000696159.1:c.348T= ENSP00000512449.1:p.Ile116=
ENST00000696160.1:c.348T= ENSP00000512450.1:p.Ile116=
ENST00000696161.1:c.478T= ENSP00000512451.1:p.Cys160=
ENST00000696162.1:c.348T= ENSP00000512452.1:p.Ile116=
ENST00000696163.1:c.297T= ENSP00000512453.1:p.Ile99=
ENST00000261623.8:c.348T= MANE Select ENSP00000261623.3:p.Ile116=
ENST00000261623.7:c.348T= ENSP00000261623.3:p.Ile116=
ENST00000563526.5:n.880T=
ENST00000565588.5:c.132T=
ENST00000566229.1:c.337T= ENSP00000457060.1:p.Cys113=
ENST00000566534.5:n.927T=
ENST00000567174.5:c.348T= ENSP00000454951.1:p.Ile116=
ENST00000568278.1:c.432T= ENSP00000455506.1:p.Ile144=
ENST00000569359.5:c.348T= ENSP00000456079.1:p.Ile116=
NM_000101.3:c.348T= NP_000092.2:p.Ile116=
XM_011522905.1:c.348T= XP_011521207.1:p.Ile116=
XM_011522905.3:c.348T= XP_011521207.1:p.Ile116=
NM_000101.4:c.348T= MANE Select NP_000092.2:p.Ile116=