Canonical Allele Identifier: CA728286034
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs1165859086

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256080_34256081insCCC , CM000679.2:g.34256080_34256081insCCC GRCh38
NC_000017.10:g.32583099_32583100insCCC , CM000679.1:g.32583099_32583100insCCC GRCh37
NC_000017.9:g.29607212_29607213insCCC NCBI36
NG_012123.1:g.5804_5805insCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.77-142_77-141insCCC ENSP00000462156.1:n.77-142_77-141insCCC
ENST00000624362.2:n.796_797insCCC
ENST00000225831.4:c.77-142_77-141insCCC MANE Select ENSP00000225831.4:n.77-142_77-141insCCC
ENST00000580907.5:c.77-142_77-141insCCC ENSP00000462156.1:n.77-142_77-141insCCC
ENST00000624362.1:n.863_864insCCC
NM_002982.3:c.77-142_77-141insCCC NP_002973.1:n.77-142_77-141insCCC
NM_002982.4:c.77-142_77-141insCCC MANE Select NP_002973.1:n.77-142_77-141insCCC