Canonical Allele Identifier: CA492499682

Gene: CHD2

Linked Data

• MyVariant Identifiers: chr15:g.93521538C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.92978308C>T , CM000677.2:g.92978308C>T	GRCh38
NC_000015.9:g.93521538C>T , CM000677.1:g.93521538C>T	GRCh37
NC_000015.8:g.91322542C>T	NCBI36
NG_012826.1:g.82988C>T
NG_012826.2:g.82988C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000625662.3:c.2159C>T
ENST00000628118.2:c.1686C>T
ENST00000700551.1:c.*1483C>T	ENSP00000515057.1:n.*1483C>T
ENST00000394196.9:c.2652C>T MANE Select	ENSP00000377747.4:p.Ile884=
ENST00000635856.1:n.3224C>T
ENST00000636306.1:n.212C>T
ENST00000636881.1:c.2023C>T
ENST00000637572.1:n.3396C>T
ENST00000394196.8:c.2652C>T	ENSP00000377747.4:p.Ile884=
ENST00000625463.1:c.192C>T	ENSP00000486391.1:p.Ile64=
ENST00000626874.2:c.2652C>T	ENSP00000486629.1:p.Ile884=
ENST00000628118.1:n.431C>T
NM_001271.3:c.2652C>T	NP_001262.3:p.Ile884=
NM_001271.4:c.2652C>T MANE Select	NP_001262.3:p.Ile884=