Canonical Allele Identifier: CA289528750
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs775202538
gnomAD v3: 17-34256450-G-A
gnomAD v4: 17-34256450-G-A
MyVariant Identifiers: chr17:g.32583469G>A (hg19) chr17:g.34256450G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256450G>A , CM000679.2:g.34256450G>A GRCh38
NC_000017.10:g.32583469G>A , CM000679.1:g.32583469G>A GRCh37
NC_000017.9:g.29607582G>A NCBI36
NG_012123.1:g.6174G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.*107G>A ENSP00000462156.1:n.*107G>A
ENST00000624362.2:n.1166G>A
ENST00000225831.4:c.194+111G>A MANE Select ENSP00000225831.4:n.194+111G>A
ENST00000580907.5:c.*107G>A ENSP00000462156.1:n.*107G>A
ENST00000582017.1:n.243G>A
NM_002982.3:c.194+111G>A NP_002973.1:n.194+111G>A
NM_002982.4:c.194+111G>A MANE Select NP_002973.1:n.194+111G>A
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