Canonical Allele Identifier: CA2256959567
Gene: CCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255415C= , CM000679.2:g.34255415C= GRCh38
NC_000017.10:g.32582434C= , CM000679.1:g.32582434C= GRCh37
NC_000017.9:g.29606547C= NCBI36
NG_012123.1:g.5139C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.66C= ENSP00000462156.1:p.Leu22=
ENST00000624362.2:n.131C=
ENST00000225831.4:c.66C= MANE Select ENSP00000225831.4:p.Leu22=
ENST00000580907.5:c.66C= ENSP00000462156.1:p.Leu22=
ENST00000624362.1:n.198C=
NM_002982.3:c.66C= NP_002973.1:p.Leu22=
NM_002982.4:c.66C= MANE Select NP_002973.1:p.Leu22=