Canonical Allele Identifier: CA397062889

Gene: CYBA

Linked Data

• MyVariant Identifiers: chr16:g.88712545A>T (hg19) ; chr16:g.88646137A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88646137A>T , CM000678.2:g.88646137A>T	GRCh38
NC_000016.9:g.88712545A>T , CM000678.1:g.88712545A>T	GRCh37
NC_000016.8:g.87240046A>T	NCBI36
NG_007291.1:g.9913T>A , LRG_52:g.9913T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000565588.6:c.348T>A	ENSP00000455537.2:p.Ile116=
ENST00000696156.1:c.264T>A	ENSP00000512446.1:p.Ile88=
ENST00000696157.1:c.348T>A	ENSP00000512447.1:p.Ile116=
ENST00000696158.1:c.348T>A	ENSP00000512448.1:p.Ile116=
ENST00000696159.1:c.348T>A	ENSP00000512449.1:p.Ile116=
ENST00000696160.1:c.348T>A	ENSP00000512450.1:p.Ile116=
ENST00000696161.1:c.478T>A	ENSP00000512451.1:p.Cys160Ser
ENST00000696162.1:c.348T>A	ENSP00000512452.1:p.Ile116=
ENST00000696163.1:c.297T>A	ENSP00000512453.1:p.Ile99=
ENST00000261623.8:c.348T>A MANE Select	ENSP00000261623.3:p.Ile116=
ENST00000261623.7:c.348T>A	ENSP00000261623.3:p.Ile116=
ENST00000563526.5:n.880T>A
ENST00000565588.5:c.132T>A
ENST00000566229.1:c.337T>A	ENSP00000457060.1:p.Cys113Ser
ENST00000566534.5:n.927T>A
ENST00000567174.5:c.348T>A	ENSP00000454951.1:p.Ile116=
ENST00000568278.1:c.432T>A	ENSP00000455506.1:p.Ile144=
ENST00000569359.5:c.348T>A	ENSP00000456079.1:p.Ile116=
NM_000101.3:c.348T>A	NP_000092.2:p.Ile116=
XM_011522905.1:c.348T>A	XP_011521207.1:p.Ile116=
XM_011522905.3:c.348T>A	XP_011521207.1:p.Ile116=
NM_000101.4:c.348T>A MANE Select	NP_000092.2:p.Ile116=