Canonical Allele Identifier: CA352465872

Gene: CCR2

Linked Data

• MyVariant Identifiers: chr3:g.46399029C>T (hg19) ; chr3:g.46357538C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46357538C>T , CM000665.2:g.46357538C>T	GRCh38
NC_000003.11:g.46399029C>T , CM000665.1:g.46399029C>T	GRCh37
NC_000003.10:g.46374033C>T	NCBI36
NG_021428.1:g.8795C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445132.3:c.11C>T MANE Select	ENSP00000399285.2:p.Thr4Ile
ENST00000292301.4:c.11C>T	ENSP00000292301.3:p.Thr4Ile
ENST00000400888.2:c.11C>T	ENSP00000383681.2:p.Thr4Ile
ENST00000421659.1:c.11C>T	ENSP00000396736.1:p.Thr4Ile
ENST00000445132.2:c.11C>T	ENSP00000399285.2:p.Thr4Ile
ENST00000465202.1:n.315-579C>T
NM_001123041.2:c.11C>T	NP_001116513.2:p.Thr4Ile
NM_001123396.1:c.11C>T	NP_001116868.1:p.Thr4Ile
XM_011534069.1:c.11C>T	XP_011532371.1:p.Thr4Ile
NM_001123396.2:c.11C>T	NP_001116868.1:p.Thr4Ile
NM_001123396.3:c.11C>T	NP_001116868.1:p.Thr4Ile
NM_001123041.3:c.11C>T	NP_001116513.2:p.Thr4Ile
NM_001123396.4:c.11C>T MANE Select	NP_001116868.1:p.Thr4Ile