Canonical Allele Identifier: CA2241201758
Gene: CYBA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88646960G= , CM000678.2:g.88646960G= GRCh38
NC_000016.9:g.88713368G= , CM000678.1:g.88713368G= GRCh37
NC_000016.8:g.87240869G= NCBI36
NG_007291.1:g.9090C= , LRG_52:g.9090C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000565588.6:c.204-122C= ENSP00000455537.2:n.204-122C=
ENST00000696156.1:c.203+141C= ENSP00000512446.1:n.203+141C=
ENST00000696157.1:c.204-122C= ENSP00000512447.1:n.204-122C=
ENST00000696158.1:c.204-122C= ENSP00000512448.1:n.204-122C=
ENST00000696159.1:c.204-122C= ENSP00000512449.1:n.204-122C=
ENST00000696160.1:c.204-122C= ENSP00000512450.1:n.204-122C=
ENST00000696161.1:c.212C= ENSP00000512451.1:p.Pro71=
ENST00000696162.1:c.204-122C= ENSP00000512452.1:n.204-122C=
ENST00000696163.1:c.203+141C= ENSP00000512453.1:n.203+141C=
ENST00000261623.8:c.204-122C= MANE Select ENSP00000261623.3:n.204-122C=
ENST00000261623.7:c.204-122C= ENSP00000261623.3:n.204-122C=
ENST00000562209.1:n.362C=
ENST00000563526.5:n.179-122C=
ENST00000566229.1:c.193-122C= ENSP00000457060.1:n.193-122C=
ENST00000566534.5:n.226-122C=
ENST00000567174.5:c.204-122C= ENSP00000454951.1:n.204-122C=
ENST00000568278.1:c.204-122C= ENSP00000455506.1:n.204-122C=
ENST00000569359.5:c.204-122C= ENSP00000456079.1:n.204-122C=
NM_000101.3:c.204-122C= NP_000092.2:n.204-122C=
XM_011522905.1:c.204-122C= XP_011521207.1:n.204-122C=
XM_011522905.3:c.204-122C= XP_011521207.1:n.204-122C=
NM_000101.4:c.204-122C= MANE Select NP_000092.2:n.204-122C=