Canonical Allele Identifier: CA499710165
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs1267707319
gnomAD v3: 17-34255249-T-C
gnomAD v4: 17-34255249-T-C
MyVariant Identifiers: chr17:g.32582268T>C (hg19) chr17:g.34255249T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255249T>C , CM000679.2:g.34255249T>C GRCh38
NC_000017.10:g.32582268T>C , CM000679.1:g.32582268T>C GRCh37
NC_000017.9:g.29606381T>C NCBI36
NG_012123.1:g.4973T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000624362.1:n.32T>C
Search 100 bp 5'
Search 100 bp 3'