Canonical Allele Identifier: CA393893609

Gene: CHD2

Linked Data

• MyVariant Identifiers: chr15:g.93518170A>C (hg19) ; chr15:g.92974940A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.92974940A>C , CM000677.2:g.92974940A>C	GRCh38
NC_000015.9:g.93518170A>C , CM000677.1:g.93518170A>C	GRCh37
NC_000015.8:g.91319174A>C	NCBI36
NG_012826.1:g.79620A>C
NG_012826.2:g.79620A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000625662.3:c.2074A>C
ENST00000628118.2:c.1515A>C
ENST00000700550.1:c.*561A>C	ENSP00000515056.1:n.*561A>C
ENST00000700551.1:c.*1398A>C	ENSP00000515057.1:n.*1398A>C
ENST00000394196.9:c.2567A>C MANE Select	ENSP00000377747.4:p.Asp856Ala
ENST00000635856.1:n.3139A>C
ENST00000636306.1:n.127A>C
ENST00000636881.1:c.1938A>C
ENST00000637572.1:n.3311A>C
ENST00000394196.8:c.2567A>C	ENSP00000377747.4:p.Asp856Ala
ENST00000625463.1:c.107A>C	ENSP00000486391.1:p.Asp36Ala
ENST00000626874.2:c.2567A>C	ENSP00000486629.1:p.Asp856Ala
ENST00000628118.1:n.260A>C
NM_001271.3:c.2567A>C	NP_001262.3:p.Asp856Ala
NM_001271.4:c.2567A>C MANE Select	NP_001262.3:p.Asp856Ala