Canonical Allele Identifier: CA2256959558
Gene: CCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255392G= , CM000679.2:g.34255392G= GRCh38
NC_000017.10:g.32582411G= , CM000679.1:g.32582411G= GRCh37
NC_000017.9:g.29606524G= NCBI36
NG_012123.1:g.5116G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.43G= ENSP00000462156.1:p.Ala15=
ENST00000624362.2:n.108G=
ENST00000225831.4:c.43G= MANE Select ENSP00000225831.4:p.Ala15=
ENST00000580907.5:c.43G= ENSP00000462156.1:p.Ala15=
ENST00000624362.1:n.175G=
NM_002982.3:c.43G= NP_002973.1:p.Ala15=
NM_002982.4:c.43G= MANE Select NP_002973.1:p.Ala15=