Canonical Allele Identifier: CA2241199514
Gene: CYBA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88643324C= , CM000678.2:g.88643324C= GRCh38
NC_000016.9:g.88709732C= , CM000678.1:g.88709732C= GRCh37
NC_000016.8:g.87237233C= NCBI36
NG_007291.1:g.12726G= , LRG_52:g.12726G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696156.1:c.*29G= ENSP00000512446.1:n.*29G=
ENST00000696157.1:c.*834G= ENSP00000512447.1:n.*834G=
ENST00000696158.1:c.*871G= ENSP00000512448.1:n.*871G=
ENST00000696159.1:c.*540G= ENSP00000512449.1:n.*540G=
ENST00000696160.1:c.*29G= ENSP00000512450.1:n.*29G=
ENST00000696161.1:c.747G= ENSP00000512451.1:p.Arg249=
ENST00000696162.1:c.*1336G= ENSP00000512452.1:n.*1336G=
ENST00000696163.1:c.*29G= ENSP00000512453.1:n.*29G=
ENST00000261623.8:c.*29G= MANE Select ENSP00000261623.3:n.*29G=
ENST00000261623.7:c.*29G= ENSP00000261623.3:n.*29G=
NM_000101.3:c.*29G= NP_000092.2:n.*29G=
NM_000101.4:c.*29G= MANE Select NP_000092.2:n.*29G=