Canonical Allele Identifier: CA2241199645
Gene: CYBA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88643428C= , CM000678.2:g.88643428C= GRCh38
NC_000016.9:g.88709836C= , CM000678.1:g.88709836C= GRCh37
NC_000016.8:g.87237337C= NCBI36
NG_007291.1:g.12622G= , LRG_52:g.12622G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696156.1:c.429G= ENSP00000512446.1:p.Glu143=
ENST00000696157.1:c.*730G= ENSP00000512447.1:n.*730G=
ENST00000696158.1:c.*767G= ENSP00000512448.1:n.*767G=
ENST00000696159.1:c.*436G= ENSP00000512449.1:n.*436G=
ENST00000696160.1:c.540G= ENSP00000512450.1:p.Glu180=
ENST00000696161.1:c.643G= ENSP00000512451.1:p.Gly215=
ENST00000696162.1:c.*1232G= ENSP00000512452.1:n.*1232G=
ENST00000696163.1:c.462G= ENSP00000512453.1:p.Glu154=
ENST00000261623.8:c.513G= MANE Select ENSP00000261623.3:p.Glu171=
ENST00000261623.7:c.513G= ENSP00000261623.3:p.Glu171=
NM_000101.3:c.513G= NP_000092.2:p.Glu171=
NM_000101.4:c.513G= MANE Select NP_000092.2:p.Glu171=