Canonical Allele Identifier: CA399059767
Gene: CCL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255401A>T , CM000679.2:g.34255401A>T GRCh38
NC_000017.10:g.32582420A>T , CM000679.1:g.32582420A>T GRCh37
NC_000017.9:g.29606533A>T NCBI36
NG_012123.1:g.5125A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.52A>T ENSP00000462156.1:p.Ile18Phe
ENST00000624362.2:n.117A>T
ENST00000225831.4:c.52A>T MANE Select ENSP00000225831.4:p.Ile18Phe
ENST00000580907.5:c.52A>T ENSP00000462156.1:p.Ile18Phe
ENST00000624362.1:n.184A>T
NM_002982.3:c.52A>T NP_002973.1:p.Ile18Phe
NM_002982.4:c.52A>T MANE Select NP_002973.1:p.Ile18Phe