Canonical Allele Identifier: CA499710235
Gene: CCL2 HGNC NCBI

Linked Data

gnomAD v4: 17-34255275-C-T
MyVariant Identifiers: chr17:g.32582294C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255275C>T , CM000679.2:g.34255275C>T GRCh38
NC_000017.10:g.32582294C>T , CM000679.1:g.32582294C>T GRCh37
NC_000017.9:g.29606407C>T NCBI36
NG_012123.1:g.4999C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.-75C>T ENSP00000462156.1:n.-75C>T
ENST00000624362.1:n.58C>T
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