Canonical Allele Identifier: CA399060230
Gene: CCL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.32583339T>A (hg19) chr17:g.34256320T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256320T>A , CM000679.2:g.34256320T>A GRCh38
NC_000017.10:g.32583339T>A , CM000679.1:g.32583339T>A GRCh37
NC_000017.9:g.29607452T>A NCBI36
NG_012123.1:g.6044T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.175T>A ENSP00000462156.1:p.Cys59Ser
ENST00000624362.2:n.1036T>A
ENST00000225831.4:c.175T>A MANE Select ENSP00000225831.4:p.Cys59Ser
ENST00000580907.5:c.175T>A ENSP00000462156.1:p.Cys59Ser
ENST00000582017.1:n.113T>A
NM_002982.3:c.175T>A NP_002973.1:p.Cys59Ser
NM_002982.4:c.175T>A MANE Select NP_002973.1:p.Cys59Ser
Search 100 bp 5'
Search 100 bp 3'