Canonical Allele Identifier: CA399059787
Gene: CCL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.32582429G>A (hg19) chr17:g.34255410G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255410G>A , CM000679.2:g.34255410G>A GRCh38
NC_000017.10:g.32582429G>A , CM000679.1:g.32582429G>A GRCh37
NC_000017.9:g.29606542G>A NCBI36
NG_012123.1:g.5134G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.61G>A ENSP00000462156.1:p.Gly21Arg
ENST00000624362.2:n.126G>A
ENST00000225831.4:c.61G>A MANE Select ENSP00000225831.4:p.Gly21Arg
ENST00000580907.5:c.61G>A ENSP00000462156.1:p.Gly21Arg
ENST00000624362.1:n.193G>A
NM_002982.3:c.61G>A NP_002973.1:p.Gly21Arg
NM_002982.4:c.61G>A MANE Select NP_002973.1:p.Gly21Arg
Search 100 bp 5'
Search 100 bp 3'