Canonical Allele Identifier: CA2196373755

Gene: CHD2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.92978254G= , CM000677.2:g.92978254G=	GRCh38
NC_000015.9:g.93521484G= , CM000677.1:g.93521484G=	GRCh37
NC_000015.8:g.91322488G=	NCBI36
NG_012826.1:g.82934G=
NG_012826.2:g.82934G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000625662.3:c.2105G=
ENST00000628118.2:c.1632G=
ENST00000700551.1:c.*1429G=	ENSP00000515057.1:n.*1429G=
ENST00000394196.9:c.2598G= MANE Select	ENSP00000377747.4:p.Ser866=
ENST00000635856.1:n.3170G=
ENST00000636306.1:n.158G=
ENST00000636881.1:c.1969G=
ENST00000637572.1:n.3342G=
ENST00000394196.8:c.2598G=	ENSP00000377747.4:p.Ser866=
ENST00000625463.1:c.138G=	ENSP00000486391.1:p.Ser46=
ENST00000626874.2:c.2598G=	ENSP00000486629.1:p.Ser866=
ENST00000628118.1:n.377G=
NM_001271.3:c.2598G=	NP_001262.3:p.Ser866=
NM_001271.4:c.2598G= MANE Select	NP_001262.3:p.Ser866=