Canonical Allele Identifier: CA2354453

Gene: CCR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46358570C>T , CM000665.2:g.46358570C>T	GRCh38
NC_000003.11:g.46400061C>T , CM000665.1:g.46400061C>T	GRCh37
NC_000003.10:g.46375065C>T	NCBI36
NG_021428.1:g.9827C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001123396.4:c.1043C>T MANE Select	NP_001116868.1:p.Thr348Met
ENST00000445132.3:c.1043C>T MANE Select	ENSP00000399285.2:p.Thr348Met
NM_001123041.2:c.941+102C>T	NP_001116513.2:n.941+102C>T
NM_001123041.3:c.941+102C>T	NP_001116513.2:n.941+102C>T
NM_001123396.1:c.1043C>T	NP_001116868.1:p.Thr348Met
NM_001123396.2:c.1043C>T	NP_001116868.1:p.Thr348Met
NM_001123396.3:c.1043C>T	NP_001116868.1:p.Thr348Met
ENST00000292301.4:c.941+102C>T	ENSP00000292301.3:n.941+102C>T
ENST00000400888.2:c.941+102C>T	ENSP00000383681.2:n.941+102C>T
ENST00000445132.2:c.1043C>T	ENSP00000399285.2:p.Thr348Met
ENST00000465202.1:n.768C>T
XM_011534069.1:c.1043C>T	XP_011532371.1:p.Thr348Met