Canonical Allele Identifier: CA399060081
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs1907682657
gnomAD v3: 17-34256278-G-A
gnomAD v4: 17-34256278-G-A
MyVariant Identifiers: chr17:g.32583297G>A (hg19) chr17:g.34256278G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256278G>A , CM000679.2:g.34256278G>A GRCh38
NC_000017.10:g.32583297G>A , CM000679.1:g.32583297G>A GRCh37
NC_000017.9:g.29607410G>A NCBI36
NG_012123.1:g.6002G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.133G>A ENSP00000462156.1:p.Val45Met
ENST00000624362.2:n.994G>A
ENST00000225831.4:c.133G>A MANE Select ENSP00000225831.4:p.Val45Met
ENST00000580907.5:c.133G>A ENSP00000462156.1:p.Val45Met
ENST00000582017.1:n.71G>A
NM_002982.3:c.133G>A NP_002973.1:p.Val45Met
NM_002982.4:c.133G>A MANE Select NP_002973.1:p.Val45Met
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