Canonical Allele Identifier: CA2241199650
Gene: CYBA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88643441G= , CM000678.2:g.88643441G= GRCh38
NC_000016.9:g.88709849G= , CM000678.1:g.88709849G= GRCh37
NC_000016.8:g.87237350G= NCBI36
NG_007291.1:g.12609C= , LRG_52:g.12609C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696156.1:c.416C= ENSP00000512446.1:p.Pro139=
ENST00000696157.1:c.*717C= ENSP00000512447.1:n.*717C=
ENST00000696158.1:c.*754C= ENSP00000512448.1:n.*754C=
ENST00000696159.1:c.*423C= ENSP00000512449.1:n.*423C=
ENST00000696160.1:c.527C= ENSP00000512450.1:p.Pro176=
ENST00000696161.1:c.630C= ENSP00000512451.1:p.Ala210=
ENST00000696162.1:c.*1219C= ENSP00000512452.1:n.*1219C=
ENST00000696163.1:c.449C= ENSP00000512453.1:p.Pro150=
ENST00000261623.8:c.500C= MANE Select ENSP00000261623.3:p.Pro167=
ENST00000261623.7:c.500C= ENSP00000261623.3:p.Pro167=
NM_000101.3:c.500C= NP_000092.2:p.Pro167=
NM_000101.4:c.500C= MANE Select NP_000092.2:p.Pro167=