Canonical Allele Identifier: CA289528511
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs3917887

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255980_34255993del , CM000679.2:g.34255980_34255993del GRCh38
NC_000017.10:g.32582999_32583012del , CM000679.1:g.32582999_32583012del GRCh37
NC_000017.9:g.29607112_29607125del NCBI36
NG_012123.1:g.5704_5717del

Transcript Alleles

HGVS Amino-acid change
ENST00000580907.6:c.77-242_77-229del ENSP00000462156.1:n.77-242_77-229del
ENST00000624362.2:n.696_709del
ENST00000225831.4:c.77-242_77-229del MANE Select ENSP00000225831.4:n.77-242_77-229del
ENST00000580907.5:c.77-242_77-229del ENSP00000462156.1:n.77-242_77-229del
ENST00000624362.1:n.763_776del
NM_002982.3:c.77-242_77-229del NP_002973.1:n.77-242_77-229del
NM_002982.4:c.77-242_77-229del MANE Select NP_002973.1:n.77-242_77-229del