Canonical Allele Identifier: CA2241199638
Gene: CYBA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88643421C= , CM000678.2:g.88643421C= GRCh38
NC_000016.9:g.88709829C= , CM000678.1:g.88709829C= GRCh37
NC_000016.8:g.87237330C= NCBI36
NG_007291.1:g.12629G= , LRG_52:g.12629G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696156.1:c.436G= ENSP00000512446.1:p.Val146=
ENST00000696157.1:c.*737G= ENSP00000512447.1:n.*737G=
ENST00000696158.1:c.*774G= ENSP00000512448.1:n.*774G=
ENST00000696159.1:c.*443G= ENSP00000512449.1:n.*443G=
ENST00000696160.1:c.547G= ENSP00000512450.1:p.Val183=
ENST00000696161.1:c.650G= ENSP00000512451.1:p.Gly217=
ENST00000696162.1:c.*1239G= ENSP00000512452.1:n.*1239G=
ENST00000696163.1:c.469G= ENSP00000512453.1:p.Val157=
ENST00000261623.8:c.520G= MANE Select ENSP00000261623.3:p.Val174=
ENST00000261623.7:c.520G= ENSP00000261623.3:p.Val174=
NM_000101.3:c.520G= NP_000092.2:p.Val174=
NM_000101.4:c.520G= MANE Select NP_000092.2:p.Val174=