Canonical Allele Identifier: CA2637210757
Gene: CCL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256486del , CM000679.2:g.34256486del GRCh38
NC_000017.10:g.32583505del , CM000679.1:g.32583505del GRCh37
NC_000017.9:g.29607618del NCBI36
NG_012123.1:g.6210del

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.*143del ENSP00000462156.1:n.*143del
ENST00000624362.2:n.1202del
ENST00000225831.4:c.194+147del MANE Select ENSP00000225831.4:n.194+147del
ENST00000580907.5:c.*143del ENSP00000462156.1:n.*143del
ENST00000582017.1:n.279del
NM_002982.3:c.194+147del NP_002973.1:n.194+147del
NM_002982.4:c.194+147del MANE Select NP_002973.1:n.194+147del