Canonical Allele Identifier: CA289528169
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs1020627118
gnomAD v2: 17-32582435-G-A
gnomAD v3: 17-34255416-G-A
gnomAD v4: 17-34255416-G-A
MyVariant Identifiers: chr17:g.32582435G>A (hg19) chr17:g.34255416G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255416G>A , CM000679.2:g.34255416G>A GRCh38
NC_000017.10:g.32582435G>A , CM000679.1:g.32582435G>A GRCh37
NC_000017.9:g.29606548G>A NCBI36
NG_012123.1:g.5140G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.67G>A ENSP00000462156.1:p.Ala23Thr
ENST00000624362.2:n.132G>A
ENST00000225831.4:c.67G>A MANE Select ENSP00000225831.4:p.Ala23Thr
ENST00000580907.5:c.67G>A ENSP00000462156.1:p.Ala23Thr
ENST00000624362.1:n.199G>A
NM_002982.3:c.67G>A NP_002973.1:p.Ala23Thr
NM_002982.4:c.67G>A MANE Select NP_002973.1:p.Ala23Thr
Search 100 bp 5'
Search 100 bp 3'