Canonical Allele Identifier: CA2241201233
Gene: CYBA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88646131G= , CM000678.2:g.88646131G= GRCh38
NC_000016.9:g.88712539G= , CM000678.1:g.88712539G= GRCh37
NC_000016.8:g.87240040G= NCBI36
NG_007291.1:g.9919C= , LRG_52:g.9919C=

Transcript Alleles

HGVS Amino-acid change
ENST00000565588.6:c.354C= ENSP00000455537.2:p.Ser118=
ENST00000696156.1:c.270C= ENSP00000512446.1:p.Ser90=
ENST00000696157.1:c.354C= ENSP00000512447.1:p.Ser118=
ENST00000696158.1:c.354C= ENSP00000512448.1:p.Ser118=
ENST00000696159.1:c.354C= ENSP00000512449.1:p.Ser118=
ENST00000696160.1:c.354C= ENSP00000512450.1:p.Ser118=
ENST00000696161.1:c.484C= ENSP00000512451.1:p.Arg162=
ENST00000696162.1:c.354C= ENSP00000512452.1:p.Ser118=
ENST00000696163.1:c.303C= ENSP00000512453.1:p.Ser101=
ENST00000261623.8:c.354C= MANE Select ENSP00000261623.3:p.Ser118=
ENST00000261623.7:c.354C= ENSP00000261623.3:p.Ser118=
ENST00000563526.5:n.886C=
ENST00000565588.5:c.138C=
ENST00000566229.1:c.343C= ENSP00000457060.1:p.Arg115=
ENST00000566534.5:n.933C=
ENST00000567174.5:c.354C= ENSP00000454951.1:p.Ser118=
ENST00000569359.5:c.354C= ENSP00000456079.1:p.Ser118=
NM_000101.3:c.354C= NP_000092.2:p.Ser118=
XM_011522905.1:c.354C= XP_011521207.1:p.Ser118=
XM_011522905.3:c.354C= XP_011521207.1:p.Ser118=
NM_000101.4:c.354C= MANE Select NP_000092.2:p.Ser118=