Canonical Allele Identifier: CA2665434505

Gene: CCR2

Linked Data

• dbSNP Id: rs2106718263
• gnomAD v4: 3-46357520-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46357520T>C , CM000665.2:g.46357520T>C	GRCh38
NC_000003.11:g.46399011T>C , CM000665.1:g.46399011T>C	GRCh37
NC_000003.10:g.46374015T>C	NCBI36
NG_021428.1:g.8777T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445132.3:c.-8T>C MANE Select	ENSP00000399285.2:n.-8T>C
ENST00000292301.4:c.-8T>C	ENSP00000292301.3:n.-8T>C
ENST00000400888.2:c.-8T>C	ENSP00000383681.2:n.-8T>C
ENST00000421659.1:c.-8T>C	ENSP00000396736.1:n.-8T>C
ENST00000445132.2:c.-8T>C	ENSP00000399285.2:n.-8T>C
ENST00000465202.1:n.315-597T>C
NM_001123041.2:c.-8T>C	NP_001116513.2:n.-8T>C
NM_001123396.1:c.-8T>C	NP_001116868.1:n.-8T>C
XM_011534069.1:c.-8T>C	XP_011532371.1:n.-8T>C
NM_001123396.2:c.-8T>C	NP_001116868.1:n.-8T>C
NM_001123396.3:c.-8T>C	NP_001116868.1:n.-8T>C
NM_001123041.3:c.-8T>C	NP_001116513.2:n.-8T>C
NM_001123396.4:c.-8T>C MANE Select	NP_001116868.1:n.-8T>C