Canonical Allele Identifier: CA2196373757

Gene: CHD2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.92978259G= , CM000677.2:g.92978259G=	GRCh38
NC_000015.9:g.93521489G= , CM000677.1:g.93521489G=	GRCh37
NC_000015.8:g.91322493G=	NCBI36
NG_012826.1:g.82939G=
NG_012826.2:g.82939G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000625662.3:c.2110G=
ENST00000628118.2:c.1637G=
ENST00000700551.1:c.*1434G=	ENSP00000515057.1:n.*1434G=
ENST00000394196.9:c.2603G= MANE Select	ENSP00000377747.4:p.Arg868=
ENST00000635856.1:n.3175G=
ENST00000636306.1:n.163G=
ENST00000636881.1:c.1974G=
ENST00000637572.1:n.3347G=
ENST00000394196.8:c.2603G=	ENSP00000377747.4:p.Arg868=
ENST00000625463.1:c.143G=	ENSP00000486391.1:p.Arg48=
ENST00000626874.2:c.2603G=	ENSP00000486629.1:p.Arg868=
ENST00000628118.1:n.382G=
NM_001271.3:c.2603G=	NP_001262.3:p.Arg868=
NM_001271.4:c.2603G= MANE Select	NP_001262.3:p.Arg868=