Canonical Allele Identifier: CA2196373728

Gene: CHD2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.92978178G= , CM000677.2:g.92978178G=	GRCh38
NC_000015.9:g.93521408G= , CM000677.1:g.93521408G=	GRCh37
NC_000015.8:g.91322412G=	NCBI36
NG_012826.1:g.82858G=
NG_012826.2:g.82858G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000625662.3:c.2085-56G=
ENST00000628118.2:c.1556G=
ENST00000700551.1:c.*1409-56G=	ENSP00000515057.1:n.*1409-56G=
ENST00000394196.9:c.2578-56G= MANE Select	ENSP00000377747.4:n.2578-56G=
ENST00000635856.1:n.3150-56G=
ENST00000636306.1:n.138-56G=
ENST00000636881.1:c.1949-56G=
ENST00000637572.1:n.3322-56G=
ENST00000394196.8:c.2578-56G=	ENSP00000377747.4:n.2578-56G=
ENST00000625463.1:c.118-56G=	ENSP00000486391.1:n.118-56G=
ENST00000626874.2:c.2578-56G=	ENSP00000486629.1:n.2578-56G=
ENST00000628118.1:n.301G=
NM_001271.3:c.2578-56G=	NP_001262.3:n.2578-56G=
NM_001271.4:c.2578-56G= MANE Select	NP_001262.3:n.2578-56G=