Canonical Allele Identifier: CA352465869

Gene: CCR2

Linked Data

• MyVariant Identifiers: chr3:g.46399028A>G (hg19) ; chr3:g.46357537A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46357537A>G , CM000665.2:g.46357537A>G	GRCh38
NC_000003.11:g.46399028A>G , CM000665.1:g.46399028A>G	GRCh37
NC_000003.10:g.46374032A>G	NCBI36
NG_021428.1:g.8794A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000445132.3:c.10A>G MANE Select	ENSP00000399285.2:p.Thr4Ala
ENST00000292301.4:c.10A>G	ENSP00000292301.3:p.Thr4Ala
ENST00000400888.2:c.10A>G	ENSP00000383681.2:p.Thr4Ala
ENST00000421659.1:c.10A>G	ENSP00000396736.1:p.Thr4Ala
ENST00000445132.2:c.10A>G	ENSP00000399285.2:p.Thr4Ala
ENST00000465202.1:n.315-580A>G
NM_001123041.2:c.10A>G	NP_001116513.2:p.Thr4Ala
NM_001123396.1:c.10A>G	NP_001116868.1:p.Thr4Ala
XM_011534069.1:c.10A>G	XP_011532371.1:p.Thr4Ala
NM_001123396.2:c.10A>G	NP_001116868.1:p.Thr4Ala
NM_001123396.3:c.10A>G	NP_001116868.1:p.Thr4Ala
NM_001123041.3:c.10A>G	NP_001116513.2:p.Thr4Ala
NM_001123396.4:c.10A>G MANE Select	NP_001116868.1:p.Thr4Ala