Canonical Allele Identifier: CA289528533
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs201264079

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255992T>A , CM000679.2:g.34255992T>A GRCh38
NC_000017.10:g.32583011T>A , CM000679.1:g.32583011T>A GRCh37
NC_000017.9:g.29607124T>A NCBI36
NG_012123.1:g.5716T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.77-230T>A ENSP00000462156.1:n.77-230T>A
ENST00000624362.2:n.708T>A
ENST00000225831.4:c.77-230T>A MANE Select ENSP00000225831.4:n.77-230T>A
ENST00000580907.5:c.77-230T>A ENSP00000462156.1:n.77-230T>A
ENST00000624362.1:n.775T>A
NM_002982.3:c.77-230T>A NP_002973.1:n.77-230T>A
NM_002982.4:c.77-230T>A MANE Select NP_002973.1:n.77-230T>A