Canonical Allele Identifier: CA433592585

Gene: CCR2

Linked Data

• gnomAD v4: 3-46357626-T-C
• MyVariant Identifiers: chr3:g.46399117T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46357626T>C , CM000665.2:g.46357626T>C	GRCh38
NC_000003.11:g.46399117T>C , CM000665.1:g.46399117T>C	GRCh37
NC_000003.10:g.46374121T>C	NCBI36
NG_021428.1:g.8883T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000445132.3:c.99T>C MANE Select	ENSP00000399285.2:p.His33=
ENST00000292301.4:c.99T>C	ENSP00000292301.3:p.His33=
ENST00000400888.2:c.99T>C	ENSP00000383681.2:p.His33=
ENST00000421659.1:c.99T>C	ENSP00000396736.1:p.His33=
ENST00000445132.2:c.99T>C	ENSP00000399285.2:p.His33=
ENST00000465202.1:n.315-491T>C
NM_001123041.2:c.99T>C	NP_001116513.2:p.His33=
NM_001123396.1:c.99T>C	NP_001116868.1:p.His33=
XM_011534069.1:c.99T>C	XP_011532371.1:p.His33=
NM_001123396.2:c.99T>C	NP_001116868.1:p.His33=
NM_001123396.3:c.99T>C	NP_001116868.1:p.His33=
NM_001123041.3:c.99T>C	NP_001116513.2:p.His33=
NM_001123396.4:c.99T>C MANE Select	NP_001116868.1:p.His33=