Canonical Allele Identifier: CA399059941
Gene: CCL2 HGNC NCBI

Linked Data

COSMIC: COSM4065460
MyVariant Identifiers: chr17:g.32583268G>A (hg19) chr17:g.34256249G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256249G>A , CM000679.2:g.34256249G>A GRCh38
NC_000017.10:g.32583268G>A , CM000679.1:g.32583268G>A GRCh37
NC_000017.9:g.29607381G>A NCBI36
NG_012123.1:g.5973G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.104G>A ENSP00000462156.1:p.Cys35Tyr
ENST00000624362.2:n.965G>A
ENST00000225831.4:c.104G>A MANE Select ENSP00000225831.4:p.Cys35Tyr
ENST00000580907.5:c.104G>A ENSP00000462156.1:p.Cys35Tyr
ENST00000582017.1:n.42G>A
NM_002982.3:c.104G>A NP_002973.1:p.Cys35Tyr
NM_002982.4:c.104G>A MANE Select NP_002973.1:p.Cys35Tyr
Search 100 bp 5'
Search 100 bp 3'