Canonical Allele Identifier: CA499710258
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs1420103519
MyVariant Identifiers: chr17:g.32582303C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255284C>A , CM000679.2:g.34255284C>A GRCh38
NC_000017.10:g.32582303C>A , CM000679.1:g.32582303C>A GRCh37
NC_000017.9:g.29606416C>A NCBI36
NG_012123.1:g.5008C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.-66C>A ENSP00000462156.1:n.-66C>A
ENST00000624362.1:n.67C>A
NM_002982.3:c.-66C>A NP_002973.1:n.-66C>A
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