Canonical Allele Identifier: CA399059812
Gene: CCL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255423C>A , CM000679.2:g.34255423C>A GRCh38
NC_000017.10:g.32582442C>A , CM000679.1:g.32582442C>A GRCh37
NC_000017.9:g.29606555C>A NCBI36
NG_012123.1:g.5147C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.74C>A ENSP00000462156.1:p.Pro25Gln
ENST00000624362.2:n.139C>A
ENST00000225831.4:c.74C>A MANE Select ENSP00000225831.4:p.Pro25Gln
ENST00000580907.5:c.74C>A ENSP00000462156.1:p.Pro25Gln
ENST00000624362.1:n.206C>A
NM_002982.3:c.74C>A NP_002973.1:p.Pro25Gln
NM_002982.4:c.74C>A MANE Select NP_002973.1:p.Pro25Gln