Canonical Allele Identifier: CA352466098

Gene: CCR2

Linked Data

• MyVariant Identifiers: chr3:g.46399115C>A (hg19) ; chr3:g.46357624C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46357624C>A , CM000665.2:g.46357624C>A	GRCh38
NC_000003.11:g.46399115C>A , CM000665.1:g.46399115C>A	GRCh37
NC_000003.10:g.46374119C>A	NCBI36
NG_021428.1:g.8881C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000445132.3:c.97C>A MANE Select	ENSP00000399285.2:p.His33Asn
ENST00000292301.4:c.97C>A	ENSP00000292301.3:p.His33Asn
ENST00000400888.2:c.97C>A	ENSP00000383681.2:p.His33Asn
ENST00000421659.1:c.97C>A	ENSP00000396736.1:p.His33Asn
ENST00000445132.2:c.97C>A	ENSP00000399285.2:p.His33Asn
ENST00000465202.1:n.315-493C>A
NM_001123041.2:c.97C>A	NP_001116513.2:p.His33Asn
NM_001123396.1:c.97C>A	NP_001116868.1:p.His33Asn
XM_011534069.1:c.97C>A	XP_011532371.1:p.His33Asn
NM_001123396.2:c.97C>A	NP_001116868.1:p.His33Asn
NM_001123396.3:c.97C>A	NP_001116868.1:p.His33Asn
NM_001123041.3:c.97C>A	NP_001116513.2:p.His33Asn
NM_001123396.4:c.97C>A MANE Select	NP_001116868.1:p.His33Asn