Canonical Allele Identifier: CA492499690

Gene: CHD2

Linked Data

• MyVariant Identifiers: chr15:g.93521556C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.92978326C>T , CM000677.2:g.92978326C>T	GRCh38
NC_000015.9:g.93521556C>T , CM000677.1:g.93521556C>T	GRCh37
NC_000015.8:g.91322560C>T	NCBI36
NG_012826.1:g.83006C>T
NG_012826.2:g.83006C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000625662.3:c.2177C>T
ENST00000628118.2:c.1704C>T
ENST00000700551.1:c.*1501C>T	ENSP00000515057.1:n.*1501C>T
ENST00000394196.9:c.2670C>T MANE Select	ENSP00000377747.4:p.Asn890=
ENST00000635856.1:n.3242C>T
ENST00000636306.1:n.230C>T
ENST00000636881.1:c.2041C>T
ENST00000637572.1:n.3414C>T
ENST00000394196.8:c.2670C>T	ENSP00000377747.4:p.Asn890=
ENST00000625463.1:c.210C>T	ENSP00000486391.1:p.Asn70=
ENST00000626874.2:c.2670C>T	ENSP00000486629.1:p.Asn890=
ENST00000628118.1:n.449C>T
NM_001271.3:c.2670C>T	NP_001262.3:p.Asn890=
NM_001271.4:c.2670C>T MANE Select	NP_001262.3:p.Asn890=