Canonical Allele Identifier: CA499710255
Gene: CCL2 HGNC NCBI

Linked Data

gnomAD v4: 17-34255283-C-T
MyVariant Identifiers: chr17:g.32582302C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255283C>T , CM000679.2:g.34255283C>T GRCh38
NC_000017.10:g.32582302C>T , CM000679.1:g.32582302C>T GRCh37
NC_000017.9:g.29606415C>T NCBI36
NG_012123.1:g.5007C>T

Transcript Alleles

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