Canonical Allele Identifier: CA728286339
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs1289811778
gnomAD v4: 17-34256395-G-A
MyVariant Identifiers: chr17:g.32583414G>A (hg19) chr17:g.34256395G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256395G>A , CM000679.2:g.34256395G>A GRCh38
NC_000017.10:g.32583414G>A , CM000679.1:g.32583414G>A GRCh37
NC_000017.9:g.29607527G>A NCBI36
NG_012123.1:g.6119G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.*52G>A ENSP00000462156.1:n.*52G>A
ENST00000624362.2:n.1111G>A
ENST00000225831.4:c.194+56G>A MANE Select ENSP00000225831.4:n.194+56G>A
ENST00000580907.5:c.*52G>A ENSP00000462156.1:n.*52G>A
ENST00000582017.1:n.188G>A
NM_002982.3:c.194+56G>A NP_002973.1:n.194+56G>A
NM_002982.4:c.194+56G>A MANE Select NP_002973.1:n.194+56G>A
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