Canonical Allele Identifier: CA2354498

Gene: CCR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46359789G>A , CM000665.2:g.46359789G>A	GRCh38
NC_000003.11:g.46401280G>A , CM000665.1:g.46401280G>A	GRCh37
NC_000003.10:g.46376284G>A	NCBI36
NG_021428.1:g.11046G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001123396.4:c.*1179G>A MANE Select	NP_001116868.1:n.*1179G>A
ENST00000445132.3:c.*1179G>A MANE Select	ENSP00000399285.2:n.*1179G>A
NM_001123041.2:c.1054G>A	NP_001116513.2:p.Asp352Asn
NM_001123041.3:c.1054G>A	NP_001116513.2:p.Asp352Asn
NM_001123396.2:c.*1179G>A	NP_001116868.1:n.*1179G>A
NM_001123396.3:c.*1179G>A	NP_001116868.1:n.*1179G>A
ENST00000292301.4:c.1054G>A	ENSP00000292301.3:p.Asp352Asn
ENST00000400888.2:c.1054G>A	ENSP00000383681.2:p.Asp352Asn
XM_011534069.1:c.*1179G>A	XP_011532371.1:n.*1179G>A