Canonical Allele Identifier: CA393893635

Gene: CHD2

Linked Data

• MyVariant Identifiers: chr15:g.93518182T>A (hg19) ; chr15:g.92974952T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.92974952T>A , CM000677.2:g.92974952T>A	GRCh38
NC_000015.9:g.93518182T>A , CM000677.1:g.93518182T>A	GRCh37
NC_000015.8:g.91319186T>A	NCBI36
NG_012826.1:g.79632T>A
NG_012826.2:g.79632T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000625662.3:c.2084+2T>A
ENST00000628118.2:c.1525+2T>A
ENST00000700550.1:c.*573T>A	ENSP00000515056.1:n.*573T>A
ENST00000700551.1:c.*1408+2T>A	ENSP00000515057.1:n.*1408+2T>A
ENST00000394196.9:c.2577+2T>A MANE Select	ENSP00000377747.4:n.2577+2T>A
ENST00000635856.1:n.3149+2T>A
ENST00000636306.1:n.137+2T>A
ENST00000636881.1:c.1948+2T>A
ENST00000637572.1:n.3321+2T>A
ENST00000394196.8:c.2577+2T>A	ENSP00000377747.4:n.2577+2T>A
ENST00000625463.1:c.117+2T>A	ENSP00000486391.1:n.117+2T>A
ENST00000626874.2:c.2577+2T>A	ENSP00000486629.1:n.2577+2T>A
ENST00000628118.1:n.270+2T>A
NM_001271.3:c.2577+2T>A	NP_001262.3:n.2577+2T>A
NM_001271.4:c.2577+2T>A MANE Select	NP_001262.3:n.2577+2T>A