Canonical Allele Identifier: CA2241201869
Gene: CYBA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88647137_88647138delinsCG , CM000678.2:g.88647137_88647138delinsCG GRCh38
NC_000016.9:g.88713545_88713546delinsCG , CM000678.1:g.88713545_88713546delinsCG GRCh37
NC_000016.8:g.87241046_87241047delinsCG NCBI36
NG_007291.1:g.8912_8913delinsCG , LRG_52:g.8912_8913delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000565588.6:c.166_167delinsCG ENSP00000455537.2:p.Arg56=
ENST00000696156.1:c.166_167delinsCG ENSP00000512446.1:p.Arg56=
ENST00000696157.1:c.166_167delinsCG ENSP00000512447.1:p.Arg56=
ENST00000696158.1:c.166_167delinsCG ENSP00000512448.1:p.Arg56=
ENST00000696159.1:c.166_167delinsCG ENSP00000512449.1:p.Arg56=
ENST00000696160.1:c.166_167delinsCG ENSP00000512450.1:p.Arg56=
ENST00000696161.1:c.166_167delinsCG ENSP00000512451.1:p.Arg56=
ENST00000696162.1:c.166_167delinsCG ENSP00000512452.1:p.Arg56=
ENST00000696163.1:c.166_167delinsCG ENSP00000512453.1:p.Arg56=
ENST00000261623.8:c.166_167delinsCG MANE Select ENSP00000261623.3:p.Arg56=
ENST00000261623.7:c.166_167delinsCG ENSP00000261623.3:p.Arg56=
ENST00000562209.1:n.184_185delinsCG
ENST00000563526.5:n.141_142delinsCG
ENST00000566229.1:c.155_156delinsCG ENSP00000457060.1:p.Pro52=
ENST00000566534.5:n.188_189delinsCG
ENST00000567174.5:c.166_167delinsCG ENSP00000454951.1:p.Arg56=
ENST00000568278.1:c.166_167delinsCG ENSP00000455506.1:p.Arg56=
ENST00000569359.5:c.166_167delinsCG ENSP00000456079.1:p.Arg56=
NM_000101.3:c.166_167delinsCG NP_000092.2:p.Arg56=
XM_011522905.1:c.166_167delinsCG XP_011521207.1:p.Arg56=
XM_011522905.3:c.166_167delinsCG XP_011521207.1:p.Arg56=
NM_000101.4:c.166_167delinsCG MANE Select NP_000092.2:p.Arg56=