Canonical Allele Identifier: CA399059727
Gene: CCL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.32582399C>G (hg19) chr17:g.34255380C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255380C>G , CM000679.2:g.34255380C>G GRCh38
NC_000017.10:g.32582399C>G , CM000679.1:g.32582399C>G GRCh37
NC_000017.9:g.29606512C>G NCBI36
NG_012123.1:g.5104C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000580907.6:c.31C>G ENSP00000462156.1:p.Leu11Val
ENST00000624362.2:n.96C>G
ENST00000225831.4:c.31C>G MANE Select ENSP00000225831.4:p.Leu11Val
ENST00000580907.5:c.31C>G ENSP00000462156.1:p.Leu11Val
ENST00000624362.1:n.163C>G
NM_002982.3:c.31C>G NP_002973.1:p.Leu11Val
NM_002982.4:c.31C>G MANE Select NP_002973.1:p.Leu11Val
Search 100 bp 5'
Search 100 bp 3'