Canonical Allele Identifier: CA1362075465

Gene: CCR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46357527C= , CM000665.2:g.46357527C=	GRCh38
NC_000003.11:g.46399018C= , CM000665.1:g.46399018C=	GRCh37
NC_000003.10:g.46374022C=	NCBI36
NG_021428.1:g.8784C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000445132.3:c.-1C= MANE Select	ENSP00000399285.2:n.-1C=
ENST00000292301.4:c.-1C=	ENSP00000292301.3:n.-1C=
ENST00000400888.2:c.-1C=	ENSP00000383681.2:n.-1C=
ENST00000421659.1:c.-1C=	ENSP00000396736.1:n.-1C=
ENST00000445132.2:c.-1C=	ENSP00000399285.2:n.-1C=
ENST00000465202.1:n.315-590C=
NM_001123041.2:c.-1C=	NP_001116513.2:n.-1C=
NM_001123396.1:c.-1C=	NP_001116868.1:n.-1C=
XM_011534069.1:c.-1C=	XP_011532371.1:n.-1C=
NM_001123396.2:c.-1C=	NP_001116868.1:n.-1C=
NM_001123396.3:c.-1C=	NP_001116868.1:n.-1C=
NM_001123041.3:c.-1C=	NP_001116513.2:n.-1C=
NM_001123396.4:c.-1C= MANE Select	NP_001116868.1:n.-1C=