Canonical Allele Identifier: CA399060070
Gene: CCL2 HGNC NCBI

Linked Data

gnomAD v4: 17-34256275-T-A
MyVariant Identifiers: chr17:g.32583294T>A (hg19) chr17:g.34256275T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256275T>A , CM000679.2:g.34256275T>A GRCh38
NC_000017.10:g.32583294T>A , CM000679.1:g.32583294T>A GRCh37
NC_000017.9:g.29607407T>A NCBI36
NG_012123.1:g.5999T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.130T>A ENSP00000462156.1:p.Ser44Thr
ENST00000624362.2:n.991T>A
ENST00000225831.4:c.130T>A MANE Select ENSP00000225831.4:p.Ser44Thr
ENST00000580907.5:c.130T>A ENSP00000462156.1:p.Ser44Thr
ENST00000582017.1:n.68T>A
NM_002982.3:c.130T>A NP_002973.1:p.Ser44Thr
NM_002982.4:c.130T>A MANE Select NP_002973.1:p.Ser44Thr
Search 100 bp 5'
Search 100 bp 3'