Canonical Allele Identifier: CA2241199483
Gene: CYBA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88643311G= , CM000678.2:g.88643311G= GRCh38
NC_000016.9:g.88709719G= , CM000678.1:g.88709719G= GRCh37
NC_000016.8:g.87237220G= NCBI36
NG_007291.1:g.12739C= , LRG_52:g.12739C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696156.1:c.*42C= ENSP00000512446.1:n.*42C=
ENST00000696157.1:c.*847C= ENSP00000512447.1:n.*847C=
ENST00000696158.1:c.*884C= ENSP00000512448.1:n.*884C=
ENST00000696159.1:c.*553C= ENSP00000512449.1:n.*553C=
ENST00000696160.1:c.*42C= ENSP00000512450.1:n.*42C=
ENST00000696161.1:c.760C= ENSP00000512451.1:p.Gln254=
ENST00000696162.1:c.*1349C= ENSP00000512452.1:n.*1349C=
ENST00000696163.1:c.*42C= ENSP00000512453.1:n.*42C=
ENST00000261623.8:c.*42C= MANE Select ENSP00000261623.3:n.*42C=
ENST00000261623.7:c.*42C= ENSP00000261623.3:n.*42C=
NM_000101.3:c.*42C= NP_000092.2:n.*42C=
NM_000101.4:c.*42C= MANE Select NP_000092.2:n.*42C=