Canonical Allele Identifier: CA2241199534
Gene: CYBA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88643332G= , CM000678.2:g.88643332G= GRCh38
NC_000016.9:g.88709740G= , CM000678.1:g.88709740G= GRCh37
NC_000016.8:g.87237241G= NCBI36
NG_007291.1:g.12718C= , LRG_52:g.12718C=

Transcript Alleles

HGVS Amino-acid change
ENST00000696156.1:c.*21C= ENSP00000512446.1:n.*21C=
ENST00000696157.1:c.*826C= ENSP00000512447.1:n.*826C=
ENST00000696158.1:c.*863C= ENSP00000512448.1:n.*863C=
ENST00000696159.1:c.*532C= ENSP00000512449.1:n.*532C=
ENST00000696160.1:c.*21C= ENSP00000512450.1:n.*21C=
ENST00000696161.1:c.739C= ENSP00000512451.1:p.Pro247=
ENST00000696162.1:c.*1328C= ENSP00000512452.1:n.*1328C=
ENST00000696163.1:c.*21C= ENSP00000512453.1:n.*21C=
ENST00000261623.8:c.*21C= MANE Select ENSP00000261623.3:n.*21C=
ENST00000261623.7:c.*21C= ENSP00000261623.3:n.*21C=
NM_000101.3:c.*21C= NP_000092.2:n.*21C=
NM_000101.4:c.*21C= MANE Select NP_000092.2:n.*21C=