Canonical Allele Identifier: CA1362075506
Gene: CCR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46357621T= , CM000665.2:g.46357621T= GRCh38
NC_000003.11:g.46399112T= , CM000665.1:g.46399112T= GRCh37
NC_000003.10:g.46374116T= NCBI36
NG_021428.1:g.8878T=

Transcript Alleles

HGVS Amino-acid change
ENST00000445132.3:c.94T= MANE Select ENSP00000399285.2:p.Cys32=
ENST00000292301.4:c.94T= ENSP00000292301.3:p.Cys32=
ENST00000400888.2:c.94T= ENSP00000383681.2:p.Cys32=
ENST00000421659.1:c.94T= ENSP00000396736.1:p.Cys32=
ENST00000445132.2:c.94T= ENSP00000399285.2:p.Cys32=
ENST00000465202.1:n.315-496T=
NM_001123041.2:c.94T= NP_001116513.2:p.Cys32=
NM_001123396.1:c.94T= NP_001116868.1:p.Cys32=
XM_011534069.1:c.94T= XP_011532371.1:p.Cys32=
NM_001123396.2:c.94T= NP_001116868.1:p.Cys32=
NM_001123396.3:c.94T= NP_001116868.1:p.Cys32=
NM_001123041.3:c.94T= NP_001116513.2:p.Cys32=
NM_001123396.4:c.94T= MANE Select NP_001116868.1:p.Cys32=