Canonical Allele Identifier: CA983184290
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs1907691464

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256521dup , CM000679.2:g.34256521dup GRCh38
NC_000017.10:g.32583540dup , CM000679.1:g.32583540dup GRCh37
NC_000017.9:g.29607653dup NCBI36
NG_012123.1:g.6245dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.*178dup ENSP00000462156.1:n.*178dup
ENST00000624362.2:n.1237dup
ENST00000225831.4:c.194+182dup MANE Select ENSP00000225831.4:n.194+182dup
ENST00000580907.5:c.*178dup ENSP00000462156.1:n.*178dup
ENST00000582017.1:n.314dup
NM_002982.3:c.194+182dup NP_002973.1:n.194+182dup
NM_002982.4:c.194+182dup MANE Select NP_002973.1:n.194+182dup