Canonical Allele Identifier: CA1362075464

Gene: CCR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46357526A= , CM000665.2:g.46357526A=	GRCh38
NC_000003.11:g.46399017A= , CM000665.1:g.46399017A=	GRCh37
NC_000003.10:g.46374021A=	NCBI36
NG_021428.1:g.8783A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445132.3:c.-2A= MANE Select	ENSP00000399285.2:n.-2A=
ENST00000292301.4:c.-2A=	ENSP00000292301.3:n.-2A=
ENST00000400888.2:c.-2A=	ENSP00000383681.2:n.-2A=
ENST00000421659.1:c.-2A=	ENSP00000396736.1:n.-2A=
ENST00000445132.2:c.-2A=	ENSP00000399285.2:n.-2A=
ENST00000465202.1:n.315-591A=
NM_001123041.2:c.-2A=	NP_001116513.2:n.-2A=
NM_001123396.1:c.-2A=	NP_001116868.1:n.-2A=
XM_011534069.1:c.-2A=	XP_011532371.1:n.-2A=
NM_001123396.2:c.-2A=	NP_001116868.1:n.-2A=
NM_001123396.3:c.-2A=	NP_001116868.1:n.-2A=
NM_001123041.3:c.-2A=	NP_001116513.2:n.-2A=
NM_001123396.4:c.-2A= MANE Select	NP_001116868.1:n.-2A=