Canonical Allele Identifier: CA289528640
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs866745401

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256268G>A , CM000679.2:g.34256268G>A GRCh38
NC_000017.10:g.32583287G>A , CM000679.1:g.32583287G>A GRCh37
NC_000017.9:g.29607400G>A NCBI36
NG_012123.1:g.5992G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.123G>A ENSP00000462156.1:p.Arg41=
ENST00000624362.2:n.984G>A
ENST00000225831.4:c.123G>A MANE Select ENSP00000225831.4:p.Arg41=
ENST00000580907.5:c.123G>A ENSP00000462156.1:p.Arg41=
ENST00000582017.1:n.61G>A
NM_002982.3:c.123G>A NP_002973.1:p.Arg41=
NM_002982.4:c.123G>A MANE Select NP_002973.1:p.Arg41=