Canonical Allele Identifier: CA73697537

Gene: CCR2

Linked Data

• dbSNP Id: rs1042578153
• gnomAD v2: 3-46399214-A-G
• gnomAD v4: 3-46357723-A-G
• MyVariant Identifiers: chr3:g.46399214A>G (hg19) ; chr3:g.46357723A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46357723A>G , CM000665.2:g.46357723A>G	GRCh38
NC_000003.11:g.46399214A>G , CM000665.1:g.46399214A>G	GRCh37
NC_000003.10:g.46374218A>G	NCBI36
NG_021428.1:g.8980A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000445132.3:c.196A>G MANE Select	ENSP00000399285.2:p.Ile66Val
ENST00000292301.4:c.196A>G	ENSP00000292301.3:p.Ile66Val
ENST00000400888.2:c.196A>G	ENSP00000383681.2:p.Ile66Val
ENST00000421659.1:c.196A>G	ENSP00000396736.1:p.Ile66Val
ENST00000445132.2:c.196A>G	ENSP00000399285.2:p.Ile66Val
ENST00000465202.1:n.315-394A>G
NM_001123041.2:c.196A>G	NP_001116513.2:p.Ile66Val
NM_001123396.1:c.196A>G	NP_001116868.1:p.Ile66Val
XM_011534069.1:c.196A>G	XP_011532371.1:p.Ile66Val
NM_001123396.2:c.196A>G	NP_001116868.1:p.Ile66Val
NM_001123396.3:c.196A>G	NP_001116868.1:p.Ile66Val
NM_001123041.3:c.196A>G	NP_001116513.2:p.Ile66Val
NM_001123396.4:c.196A>G MANE Select	NP_001116868.1:p.Ile66Val