Canonical Allele Identifier: CA2241201885

Gene: CYBA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88647163C= , CM000678.2:g.88647163C=	GRCh38
NC_000016.9:g.88713571C= , CM000678.1:g.88713571C=	GRCh37
NC_000016.8:g.87241072C=	NCBI36
NG_007291.1:g.8887G= , LRG_52:g.8887G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000565588.6:c.141G=	ENSP00000455537.2:p.Val47=
ENST00000696156.1:c.141G=	ENSP00000512446.1:p.Val47=
ENST00000696157.1:c.141G=	ENSP00000512447.1:p.Val47=
ENST00000696158.1:c.141G=	ENSP00000512448.1:p.Val47=
ENST00000696159.1:c.141G=	ENSP00000512449.1:p.Val47=
ENST00000696160.1:c.141G=	ENSP00000512450.1:p.Val47=
ENST00000696161.1:c.141G=	ENSP00000512451.1:p.Val47=
ENST00000696162.1:c.141G=	ENSP00000512452.1:p.Val47=
ENST00000696163.1:c.141G=	ENSP00000512453.1:p.Val47=
ENST00000261623.8:c.141G= MANE Select	ENSP00000261623.3:p.Val47=
ENST00000261623.7:c.141G=	ENSP00000261623.3:p.Val47=
ENST00000562209.1:n.159G=
ENST00000563526.5:n.116G=
ENST00000566229.1:c.130G=	ENSP00000457060.1:p.Val44=
ENST00000566534.5:n.163G=
ENST00000567174.5:c.141G=	ENSP00000454951.1:p.Val47=
ENST00000568278.1:c.141G=	ENSP00000455506.1:p.Val47=
ENST00000569359.5:c.141G=	ENSP00000456079.1:p.Val47=
NM_000101.3:c.141G=	NP_000092.2:p.Val47=
XM_011522905.1:c.141G=	XP_011521207.1:p.Val47=
XM_011522905.3:c.141G=	XP_011521207.1:p.Val47=
NM_000101.4:c.141G= MANE Select	NP_000092.2:p.Val47=