Canonical Allele Identifier: CA8495399
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs774337603
ExAC: 17:32582359 C / G
gnomAD v2: 17-32582359-C-G
gnomAD v3: 17-34255340-C-G
gnomAD v4: 17-34255340-C-G
MyVariant Identifiers: chr17:g.32582359C>G (hg19) chr17:g.34255340C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255340C>G , CM000679.2:g.34255340C>G GRCh38
NC_000017.10:g.32582359C>G , CM000679.1:g.32582359C>G GRCh37
NC_000017.9:g.29606472C>G NCBI36
NG_012123.1:g.5064C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.-10C>G ENSP00000462156.1:n.-10C>G
ENST00000624362.2:n.56C>G
ENST00000225831.4:c.-10C>G MANE Select ENSP00000225831.4:n.-10C>G
ENST00000580907.5:c.-10C>G ENSP00000462156.1:n.-10C>G
ENST00000624362.1:n.123C>G
NM_002982.3:c.-10C>G NP_002973.1:n.-10C>G
NM_002982.4:c.-10C>G MANE Select NP_002973.1:n.-10C>G
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