Canonical Allele Identifier: CA2256960051
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs1907690102

Genomic Alleles

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

Transcript Alleles

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