Canonical Allele Identifier: CA2241199575
Gene: CYBA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88643347G= , CM000678.2:g.88643347G= GRCh38
NC_000016.9:g.88709755G= , CM000678.1:g.88709755G= GRCh37
NC_000016.8:g.87237256G= NCBI36
NG_007291.1:g.12703C= , LRG_52:g.12703C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696156.1:c.*6C= ENSP00000512446.1:n.*6C=
ENST00000696157.1:c.*811C= ENSP00000512447.1:n.*811C=
ENST00000696158.1:c.*848C= ENSP00000512448.1:n.*848C=
ENST00000696159.1:c.*517C= ENSP00000512449.1:n.*517C=
ENST00000696160.1:c.*6C= ENSP00000512450.1:n.*6C=
ENST00000696161.1:c.724C= ENSP00000512451.1:p.Pro242=
ENST00000696162.1:c.*1313C= ENSP00000512452.1:n.*1313C=
ENST00000696163.1:c.*6C= ENSP00000512453.1:n.*6C=
ENST00000261623.8:c.*6C= MANE Select ENSP00000261623.3:n.*6C=
ENST00000261623.7:c.*6C= ENSP00000261623.3:n.*6C=
NM_000101.3:c.*6C= NP_000092.2:n.*6C=
NM_000101.4:c.*6C= MANE Select NP_000092.2:n.*6C=