Canonical Allele Identifier: CA2637210660
Gene: CCL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256201del , CM000679.2:g.34256201del GRCh38
NC_000017.10:g.32583220del , CM000679.1:g.32583220del GRCh37
NC_000017.9:g.29607333del NCBI36
NG_012123.1:g.5925del

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.77-21del ENSP00000462156.1:n.77-21del
ENST00000624362.2:n.917del
ENST00000225831.4:c.77-21del MANE Select ENSP00000225831.4:n.77-21del
ENST00000580907.5:c.77-21del ENSP00000462156.1:n.77-21del
ENST00000624362.1:n.984del
NM_002982.3:c.77-21del NP_002973.1:n.77-21del
NM_002982.4:c.77-21del MANE Select NP_002973.1:n.77-21del