Canonical Allele Identifier: CA8495424
Gene: CCL2 HGNC NCBI
MyVariant.info:
GRCh38 chr17:g.34255475T>A
GRCh37 chr17:g.32582494T>A
gnomAD v2:
17:32582494 T / A
gnomAD v3:
17:34255475 T / A
gnomAD v4:
chr17-34255475-T-A
Joint Max Group AF 0.0383899 (SAS)
Genomes Max Group AF 0.03485022 (SAS)
Exomes Max Group AF 0.03836087 (SAS)
dbSNP:
28730833
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255475T>A , CM000679.2:g.34255475T>A GRCh38
NC_000017.10:g.32582494T>A , CM000679.1:g.32582494T>A GRCh37
NC_000017.9:g.29606607T>A NCBI36
NG_012123.1:g.5199T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.76+50T>A ENSP00000462156.1:n.76+50T>A
ENST00000624362.2:n.191T>A
ENST00000225831.4:c.76+50T>A MANE Select ENSP00000225831.4:n.76+50T>A
ENST00000580907.5:c.76+50T>A ENSP00000462156.1:n.76+50T>A
ENST00000624362.1:n.258T>A
NM_002982.3:c.76+50T>A NP_002973.1:n.76+50T>A
NM_002982.4:c.76+50T>A MANE Select NP_002973.1:n.76+50T>A
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