Canonical Allele Identifier: CA8495381
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs751464334
ExAC: 17:32582293 C / T
gnomAD v2: 17-32582293-C-T
MyVariant Identifiers: chr17:g.32582293C>T (hg19) chr17:g.34255274C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255274C>T , CM000679.2:g.34255274C>T GRCh38
NC_000017.10:g.32582293C>T , CM000679.1:g.32582293C>T GRCh37
NC_000017.9:g.29606406C>T NCBI36
NG_012123.1:g.4998C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.-76C>T ENSP00000462156.1:n.-76C>T
ENST00000624362.1:n.57C>T
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