Canonical Allele Identifier: CA2241199602
Gene: CYBA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88643378A= , CM000678.2:g.88643378A= GRCh38
NC_000016.9:g.88709786A= , CM000678.1:g.88709786A= GRCh37
NC_000016.8:g.87237287A= NCBI36
NG_007291.1:g.12672T= , LRG_52:g.12672T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696156.1:c.479T= ENSP00000512446.1:p.Ile160=
ENST00000696157.1:c.*780T= ENSP00000512447.1:n.*780T=
ENST00000696158.1:c.*817T= ENSP00000512448.1:n.*817T=
ENST00000696159.1:c.*486T= ENSP00000512449.1:n.*486T=
ENST00000696160.1:c.590T= ENSP00000512450.1:p.Ile197=
ENST00000696161.1:c.693T= ENSP00000512451.1:p.His231=
ENST00000696162.1:c.*1282T= ENSP00000512452.1:n.*1282T=
ENST00000696163.1:c.512T= ENSP00000512453.1:p.Ile171=
ENST00000261623.8:c.563T= MANE Select ENSP00000261623.3:p.Ile188=
ENST00000261623.7:c.563T= ENSP00000261623.3:p.Ile188=
NM_000101.3:c.563T= NP_000092.2:p.Ile188=
NM_000101.4:c.563T= MANE Select NP_000092.2:p.Ile188=