Canonical Allele Identifier: CA399059734
Gene: CCL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.32582403T>A (hg19) chr17:g.34255384T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255384T>A , CM000679.2:g.34255384T>A GRCh38
NC_000017.10:g.32582403T>A , CM000679.1:g.32582403T>A GRCh37
NC_000017.9:g.29606516T>A NCBI36
NG_012123.1:g.5108T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000580907.6:c.35T>A ENSP00000462156.1:p.Leu12His
ENST00000624362.2:n.100T>A
ENST00000225831.4:c.35T>A MANE Select ENSP00000225831.4:p.Leu12His
ENST00000580907.5:c.35T>A ENSP00000462156.1:p.Leu12His
ENST00000624362.1:n.167T>A
NM_002982.3:c.35T>A NP_002973.1:p.Leu12His
NM_002982.4:c.35T>A MANE Select NP_002973.1:p.Leu12His
Search 100 bp 5'
Search 100 bp 3'