Canonical Allele Identifier: CA8495376
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs764986697
ExAC: 17:32582280 G / A
gnomAD v2: 17-32582280-G-A
gnomAD v3: 17-34255261-G-A
gnomAD v4: 17-34255261-G-A
MyVariant Identifiers: chr17:g.32582280G>A (hg19) chr17:g.34255261G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255261G>A , CM000679.2:g.34255261G>A GRCh38
NC_000017.10:g.32582280G>A , CM000679.1:g.32582280G>A GRCh37
NC_000017.9:g.29606393G>A NCBI36
NG_012123.1:g.4985G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000624362.1:n.44G>A
Search 100 bp 5'
Search 100 bp 3'