Canonical Allele Identifier: CA8495415
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs373061777
ExAC: 17:32582456 T / G
gnomAD v2: 17-32582456-T-G
gnomAD v3: 17-34255437-T-G
gnomAD v4: 17-34255437-T-G
MyVariant Identifiers: chr17:g.32582456T>G (hg19) chr17:g.34255437T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255437T>G , CM000679.2:g.34255437T>G GRCh38
NC_000017.10:g.32582456T>G , CM000679.1:g.32582456T>G GRCh37
NC_000017.9:g.29606569T>G NCBI36
NG_012123.1:g.5161T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.76+12T>G ENSP00000462156.1:n.76+12T>G
ENST00000624362.2:n.153T>G
ENST00000225831.4:c.76+12T>G MANE Select ENSP00000225831.4:n.76+12T>G
ENST00000580907.5:c.76+12T>G ENSP00000462156.1:n.76+12T>G
ENST00000624362.1:n.220T>G
NM_002982.3:c.76+12T>G NP_002973.1:n.76+12T>G
NM_002982.4:c.76+12T>G MANE Select NP_002973.1:n.76+12T>G
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