Canonical Allele Identifier: CA2196373764

Gene: CHD2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.92978298C= , CM000677.2:g.92978298C=	GRCh38
NC_000015.9:g.93521528C= , CM000677.1:g.93521528C=	GRCh37
NC_000015.8:g.91322532C=	NCBI36
NG_012826.1:g.82978C=
NG_012826.2:g.82978C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000625662.3:c.2149C=
ENST00000628118.2:c.1676C=
ENST00000700551.1:c.*1473C=	ENSP00000515057.1:n.*1473C=
ENST00000394196.9:c.2642C= MANE Select	ENSP00000377747.4:p.Thr881=
ENST00000635856.1:n.3214C=
ENST00000636306.1:n.202C=
ENST00000636881.1:c.2013C=
ENST00000637572.1:n.3386C=
ENST00000394196.8:c.2642C=	ENSP00000377747.4:p.Thr881=
ENST00000625463.1:c.182C=	ENSP00000486391.1:p.Thr61=
ENST00000626874.2:c.2642C=	ENSP00000486629.1:p.Thr881=
ENST00000628118.1:n.421C=
NM_001271.3:c.2642C=	NP_001262.3:p.Thr881=
NM_001271.4:c.2642C= MANE Select	NP_001262.3:p.Thr881=