Canonical Allele Identifier: CA2196373729

Gene: CHD2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.92978180G= , CM000677.2:g.92978180G=	GRCh38
NC_000015.9:g.93521410G= , CM000677.1:g.93521410G=	GRCh37
NC_000015.8:g.91322414G=	NCBI36
NG_012826.1:g.82860G=
NG_012826.2:g.82860G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000625662.3:c.2085-54G=
ENST00000628118.2:c.1558G=
ENST00000700551.1:c.*1409-54G=	ENSP00000515057.1:n.*1409-54G=
ENST00000394196.9:c.2578-54G= MANE Select	ENSP00000377747.4:n.2578-54G=
ENST00000635856.1:n.3150-54G=
ENST00000636306.1:n.138-54G=
ENST00000636881.1:c.1949-54G=
ENST00000637572.1:n.3322-54G=
ENST00000394196.8:c.2578-54G=	ENSP00000377747.4:n.2578-54G=
ENST00000625463.1:c.118-54G=	ENSP00000486391.1:n.118-54G=
ENST00000626874.2:c.2578-54G=	ENSP00000486629.1:n.2578-54G=
ENST00000628118.1:n.303G=
NM_001271.3:c.2578-54G=	NP_001262.3:n.2578-54G=
NM_001271.4:c.2578-54G= MANE Select	NP_001262.3:n.2578-54G=