Canonical Allele Identifier: CA393893913

Gene: CHD2

Linked Data

• MyVariant Identifiers: chr15:g.93521582C>T (hg19) ; chr15:g.92978352C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.92978352C>T , CM000677.2:g.92978352C>T	GRCh38
NC_000015.9:g.93521582C>T , CM000677.1:g.93521582C>T	GRCh37
NC_000015.8:g.91322586C>T	NCBI36
NG_012826.1:g.83032C>T
NG_012826.2:g.83032C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000625662.3:c.2203C>T
ENST00000628118.2:c.1730C>T
ENST00000700551.1:c.*1527C>T	ENSP00000515057.1:n.*1527C>T
ENST00000394196.9:c.2696C>T MANE Select	ENSP00000377747.4:p.Ala899Val
ENST00000635856.1:n.3268C>T
ENST00000636306.1:n.256C>T
ENST00000636881.1:c.2067C>T
ENST00000637572.1:n.3440C>T
ENST00000394196.8:c.2696C>T	ENSP00000377747.4:p.Ala899Val
ENST00000625463.1:c.236C>T	ENSP00000486391.1:p.Ala79Val
ENST00000626874.2:c.2696C>T	ENSP00000486629.1:p.Ala899Val
ENST00000628118.1:n.475C>T
NM_001271.3:c.2696C>T	NP_001262.3:p.Ala899Val
NM_001271.4:c.2696C>T MANE Select	NP_001262.3:p.Ala899Val