Canonical Allele Identifier: CA8495373
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs772062774
ExAC: 17:32582272 A / G
gnomAD v2: 17-32582272-A-G
gnomAD v3: 17-34255253-A-G
gnomAD v4: 17-34255253-A-G
MyVariant Identifiers: chr17:g.32582272A>G (hg19) chr17:g.34255253A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255253A>G , CM000679.2:g.34255253A>G GRCh38
NC_000017.10:g.32582272A>G , CM000679.1:g.32582272A>G GRCh37
NC_000017.9:g.29606385A>G NCBI36
NG_012123.1:g.4977A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000624362.1:n.36A>G
Search 100 bp 5'
Search 100 bp 3'