Canonical Allele Identifier: CA2241199551
Gene: CYBA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88643337C= , CM000678.2:g.88643337C= GRCh38
NC_000016.9:g.88709745C= , CM000678.1:g.88709745C= GRCh37
NC_000016.8:g.87237246C= NCBI36
NG_007291.1:g.12713G= , LRG_52:g.12713G=

Transcript Alleles

HGVS Amino-acid change
ENST00000696156.1:c.*16G= ENSP00000512446.1:n.*16G=
ENST00000696157.1:c.*821G= ENSP00000512447.1:n.*821G=
ENST00000696158.1:c.*858G= ENSP00000512448.1:n.*858G=
ENST00000696159.1:c.*527G= ENSP00000512449.1:n.*527G=
ENST00000696160.1:c.*16G= ENSP00000512450.1:n.*16G=
ENST00000696161.1:c.734G= ENSP00000512451.1:p.Cys245=
ENST00000696162.1:c.*1323G= ENSP00000512452.1:n.*1323G=
ENST00000696163.1:c.*16G= ENSP00000512453.1:n.*16G=
ENST00000261623.8:c.*16G= MANE Select ENSP00000261623.3:n.*16G=
ENST00000261623.7:c.*16G= ENSP00000261623.3:n.*16G=
NM_000101.3:c.*16G= NP_000092.2:n.*16G=
NM_000101.4:c.*16G= MANE Select NP_000092.2:n.*16G=