Canonical Allele Identifier: CA1362075544

Gene: CCR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46357717G= , CM000665.2:g.46357717G=	GRCh38
NC_000003.11:g.46399208G= , CM000665.1:g.46399208G=	GRCh37
NC_000003.10:g.46374212G=	NCBI36
NG_021428.1:g.8974G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445132.3:c.190G= MANE Select	ENSP00000399285.2:p.Val64=
ENST00000292301.4:c.190G=	ENSP00000292301.3:p.Val64=
ENST00000400888.2:c.190G=	ENSP00000383681.2:p.Val64=
ENST00000421659.1:c.190G=	ENSP00000396736.1:p.Val64=
ENST00000445132.2:c.190G=	ENSP00000399285.2:p.Val64=
ENST00000465202.1:n.315-400G=
NM_001123041.2:c.190G=	NP_001116513.2:p.Val64=
NM_001123396.1:c.190G=	NP_001116868.1:p.Val64=
XM_011534069.1:c.190G=	XP_011532371.1:p.Val64=
NM_001123396.2:c.190G=	NP_001116868.1:p.Val64=
NM_001123396.3:c.190G=	NP_001116868.1:p.Val64=
NM_001123041.3:c.190G=	NP_001116513.2:p.Val64=
NM_001123396.4:c.190G= MANE Select	NP_001116868.1:p.Val64=