Canonical Allele Identifier: CA492499649

Gene: CHD2

Linked Data

• MyVariant Identifiers: chr15:g.93521496T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.92978266T>G , CM000677.2:g.92978266T>G	GRCh38
NC_000015.9:g.93521496T>G , CM000677.1:g.93521496T>G	GRCh37
NC_000015.8:g.91322500T>G	NCBI36
NG_012826.1:g.82946T>G
NG_012826.2:g.82946T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000625662.3:c.2117T>G
ENST00000628118.2:c.1644T>G
ENST00000700551.1:c.*1441T>G	ENSP00000515057.1:n.*1441T>G
ENST00000394196.9:c.2610T>G MANE Select	ENSP00000377747.4:p.Gly870=
ENST00000635856.1:n.3182T>G
ENST00000636306.1:n.170T>G
ENST00000636881.1:c.1981T>G
ENST00000637572.1:n.3354T>G
ENST00000394196.8:c.2610T>G	ENSP00000377747.4:p.Gly870=
ENST00000625463.1:c.150T>G	ENSP00000486391.1:p.Gly50=
ENST00000626874.2:c.2610T>G	ENSP00000486629.1:p.Gly870=
ENST00000628118.1:n.389T>G
NM_001271.3:c.2610T>G	NP_001262.3:p.Gly870=
NM_001271.4:c.2610T>G MANE Select	NP_001262.3:p.Gly870=