Canonical Allele Identifier: CA15909283
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs2857657

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256113G>C , CM000679.2:g.34256113G>C GRCh38
NC_000017.10:g.32583132G>C , CM000679.1:g.32583132G>C GRCh37
NC_000017.9:g.29607245G>C NCBI36
NG_012123.1:g.5837G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000580907.6:c.77-109G>C ENSP00000462156.1:n.77-109G>C
ENST00000624362.2:n.829G>C
ENST00000225831.4:c.77-109G>C MANE Select ENSP00000225831.4:n.77-109G>C
ENST00000580907.5:c.77-109G>C ENSP00000462156.1:n.77-109G>C
ENST00000624362.1:n.896G>C
NM_002982.3:c.77-109G>C NP_002973.1:n.77-109G>C
NM_002982.4:c.77-109G>C MANE Select NP_002973.1:n.77-109G>C