Canonical Allele Identifier: CA499710304
Gene: CCL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.32582413C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255394C>A , CM000679.2:g.34255394C>A GRCh38
NC_000017.10:g.32582413C>A , CM000679.1:g.32582413C>A GRCh37
NC_000017.9:g.29606526C>A NCBI36
NG_012123.1:g.5118C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.45C>A ENSP00000462156.1:p.Ala15=
ENST00000624362.2:n.110C>A
ENST00000225831.4:c.45C>A MANE Select ENSP00000225831.4:p.Ala15=
ENST00000580907.5:c.45C>A ENSP00000462156.1:p.Ala15=
ENST00000624362.1:n.177C>A
NM_002982.3:c.45C>A NP_002973.1:p.Ala15=
NM_002982.4:c.45C>A MANE Select NP_002973.1:p.Ala15=
Search 100 bp 5'
Search 100 bp 3'