Canonical Allele Identifier: CA2576229496
Gene: CCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256378T>C , CM000679.2:g.34256378T>C GRCh38
NC_000017.10:g.32583397T>C , CM000679.1:g.32583397T>C GRCh37
NC_000017.9:g.29607510T>C NCBI36
NG_012123.1:g.6102T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.*35T>C ENSP00000462156.1:n.*35T>C
ENST00000624362.2:n.1094T>C
ENST00000225831.4:c.194+39T>C MANE Select ENSP00000225831.4:n.194+39T>C
ENST00000580907.5:c.*35T>C ENSP00000462156.1:n.*35T>C
ENST00000582017.1:n.171T>C
NM_002982.3:c.194+39T>C NP_002973.1:n.194+39T>C
NM_002982.4:c.194+39T>C MANE Select NP_002973.1:n.194+39T>C