Canonical Allele Identifier: CA2241201240
Gene: CYBA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88646142C= , CM000678.2:g.88646142C= GRCh38
NC_000016.9:g.88712550C= , CM000678.1:g.88712550C= GRCh37
NC_000016.8:g.87240051C= NCBI36
NG_007291.1:g.9908G= , LRG_52:g.9908G=

Transcript Alleles

HGVS Amino-acid change
ENST00000565588.6:c.343G= ENSP00000455537.2:p.Ala115=
ENST00000696156.1:c.259G= ENSP00000512446.1:p.Ala87=
ENST00000696157.1:c.343G= ENSP00000512447.1:p.Ala115=
ENST00000696158.1:c.343G= ENSP00000512448.1:p.Ala115=
ENST00000696159.1:c.343G= ENSP00000512449.1:p.Ala115=
ENST00000696160.1:c.343G= ENSP00000512450.1:p.Ala115=
ENST00000696161.1:c.473G= ENSP00000512451.1:p.Gly158=
ENST00000696162.1:c.343G= ENSP00000512452.1:p.Ala115=
ENST00000696163.1:c.292G= ENSP00000512453.1:p.Ala98=
ENST00000261623.8:c.343G= MANE Select ENSP00000261623.3:p.Ala115=
ENST00000261623.7:c.343G= ENSP00000261623.3:p.Ala115=
ENST00000562209.1:n.623G=
ENST00000563526.5:n.875G=
ENST00000565588.5:c.127G=
ENST00000566229.1:c.332G= ENSP00000457060.1:p.Gly111=
ENST00000566534.5:n.922G=
ENST00000567174.5:c.343G= ENSP00000454951.1:p.Ala115=
ENST00000568278.1:c.427G= ENSP00000455506.1:p.Ala143=
ENST00000569359.5:c.343G= ENSP00000456079.1:p.Ala115=
NM_000101.3:c.343G= NP_000092.2:p.Ala115=
XM_011522905.1:c.343G= XP_011521207.1:p.Ala115=
XM_011522905.3:c.343G= XP_011521207.1:p.Ala115=
NM_000101.4:c.343G= MANE Select NP_000092.2:p.Ala115=