Canonical Allele Identifier: CA399060287
Gene: CCL2 HGNC NCBI

Linked Data

gnomAD v4: 17-34256331-A-T
MyVariant Identifiers: chr17:g.32583350A>T (hg19) chr17:g.34256331A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256331A>T , CM000679.2:g.34256331A>T GRCh38
NC_000017.10:g.32583350A>T , CM000679.1:g.32583350A>T GRCh37
NC_000017.9:g.29607463A>T NCBI36
NG_012123.1:g.6055A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.186A>T ENSP00000462156.1:p.Glu62Asp
ENST00000624362.2:n.1047A>T
ENST00000225831.4:c.186A>T MANE Select ENSP00000225831.4:p.Glu62Asp
ENST00000580907.5:c.186A>T ENSP00000462156.1:p.Glu62Asp
ENST00000582017.1:n.124A>T
NM_002982.3:c.186A>T NP_002973.1:p.Glu62Asp
NM_002982.4:c.186A>T MANE Select NP_002973.1:p.Glu62Asp
Search 100 bp 5'
Search 100 bp 3'