Canonical Allele Identifier: CA399059745
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs1907654026
gnomAD v4: 17-34255390-C-A
MyVariant Identifiers: chr17:g.32582409C>A (hg19) chr17:g.34255390C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255390C>A , CM000679.2:g.34255390C>A GRCh38
NC_000017.10:g.32582409C>A , CM000679.1:g.32582409C>A GRCh37
NC_000017.9:g.29606522C>A NCBI36
NG_012123.1:g.5114C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.41C>A ENSP00000462156.1:p.Ala14Glu
ENST00000624362.2:n.106C>A
ENST00000225831.4:c.41C>A MANE Select ENSP00000225831.4:p.Ala14Glu
ENST00000580907.5:c.41C>A ENSP00000462156.1:p.Ala14Glu
ENST00000624362.1:n.173C>A
NM_002982.3:c.41C>A NP_002973.1:p.Ala14Glu
NM_002982.4:c.41C>A MANE Select NP_002973.1:p.Ala14Glu
Search 100 bp 5'
Search 100 bp 3'