Canonical Allele Identifier: CA289528601
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs748759159
gnomAD v2: 17-32583213-T-C
MyVariant Identifiers: chr17:g.32583213T>C (hg19) chr17:g.34256194T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256194T>C , CM000679.2:g.34256194T>C GRCh38
NC_000017.10:g.32583213T>C , CM000679.1:g.32583213T>C GRCh37
NC_000017.9:g.29607326T>C NCBI36
NG_012123.1:g.5918T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000580907.6:c.77-28T>C ENSP00000462156.1:n.77-28T>C
ENST00000624362.2:n.910T>C
ENST00000225831.4:c.77-28T>C MANE Select ENSP00000225831.4:n.77-28T>C
ENST00000580907.5:c.77-28T>C ENSP00000462156.1:n.77-28T>C
ENST00000624362.1:n.977T>C
NM_002982.3:c.77-28T>C NP_002973.1:n.77-28T>C
NM_002982.4:c.77-28T>C MANE Select NP_002973.1:n.77-28T>C
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