Canonical Allele Identifier: CA499710228
Gene: CCL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.32582291A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255272A>T , CM000679.2:g.34255272A>T GRCh38
NC_000017.10:g.32582291A>T , CM000679.1:g.32582291A>T GRCh37
NC_000017.9:g.29606404A>T NCBI36
NG_012123.1:g.4996A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000624362.1:n.55A>T
Search 100 bp 5'
Search 100 bp 3'