Canonical Allele Identifier: CA399059804
Gene: CCL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255420A>C , CM000679.2:g.34255420A>C GRCh38
NC_000017.10:g.32582439A>C , CM000679.1:g.32582439A>C GRCh37
NC_000017.9:g.29606552A>C NCBI36
NG_012123.1:g.5144A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.71A>C ENSP00000462156.1:p.Gln24Pro
ENST00000624362.2:n.136A>C
ENST00000225831.4:c.71A>C MANE Select ENSP00000225831.4:p.Gln24Pro
ENST00000580907.5:c.71A>C ENSP00000462156.1:p.Gln24Pro
ENST00000624362.1:n.203A>C
NM_002982.3:c.71A>C NP_002973.1:p.Gln24Pro
NM_002982.4:c.71A>C MANE Select NP_002973.1:p.Gln24Pro