Canonical Allele Identifier: CA2241199595
Gene: CYBA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88643367C= , CM000678.2:g.88643367C= GRCh38
NC_000016.9:g.88709775C= , CM000678.1:g.88709775C= GRCh37
NC_000016.8:g.87237276C= NCBI36
NG_007291.1:g.12683G= , LRG_52:g.12683G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696156.1:c.490G= ENSP00000512446.1:p.Asp164=
ENST00000696157.1:c.*791G= ENSP00000512447.1:n.*791G=
ENST00000696158.1:c.*828G= ENSP00000512448.1:n.*828G=
ENST00000696159.1:c.*497G= ENSP00000512449.1:n.*497G=
ENST00000696160.1:c.601G= ENSP00000512450.1:p.Asp201=
ENST00000696161.1:c.704G= ENSP00000512451.1:p.Arg235=
ENST00000696162.1:c.*1293G= ENSP00000512452.1:n.*1293G=
ENST00000696163.1:c.523G= ENSP00000512453.1:p.Asp175=
ENST00000261623.8:c.574G= MANE Select ENSP00000261623.3:p.Asp192=
ENST00000261623.7:c.574G= ENSP00000261623.3:p.Asp192=
NM_000101.3:c.574G= NP_000092.2:p.Asp192=
NM_000101.4:c.574G= MANE Select NP_000092.2:p.Asp192=