Canonical Allele Identifier: CA8495450
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs367586228
ExAC: 17:32583373 C / T
gnomAD v2: 17-32583373-C-T
gnomAD v3: 17-34256354-C-T
gnomAD v4: 17-34256354-C-T
MyVariant Identifiers: chr17:g.32583373C>T (hg19) chr17:g.34256354C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256354C>T , CM000679.2:g.34256354C>T GRCh38
NC_000017.10:g.32583373C>T , CM000679.1:g.32583373C>T GRCh37
NC_000017.9:g.29607486C>T NCBI36
NG_012123.1:g.6078C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.*11C>T ENSP00000462156.1:n.*11C>T
ENST00000624362.2:n.1070C>T
ENST00000225831.4:c.194+15C>T MANE Select ENSP00000225831.4:n.194+15C>T
ENST00000580907.5:c.*11C>T ENSP00000462156.1:n.*11C>T
ENST00000582017.1:n.147C>T
NM_002982.3:c.194+15C>T NP_002973.1:n.194+15C>T
NM_002982.4:c.194+15C>T MANE Select NP_002973.1:n.194+15C>T
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