Canonical Allele Identifier: CA399060033
Gene: CCL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.32583286G>T (hg19) chr17:g.34256267G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256267G>T , CM000679.2:g.34256267G>T GRCh38
NC_000017.10:g.32583286G>T , CM000679.1:g.32583286G>T GRCh37
NC_000017.9:g.29607399G>T NCBI36
NG_012123.1:g.5991G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000580907.6:c.122G>T ENSP00000462156.1:p.Arg41Met
ENST00000624362.2:n.983G>T
ENST00000225831.4:c.122G>T MANE Select ENSP00000225831.4:p.Arg41Met
ENST00000580907.5:c.122G>T ENSP00000462156.1:p.Arg41Met
ENST00000582017.1:n.60G>T
NM_002982.3:c.122G>T NP_002973.1:p.Arg41Met
NM_002982.4:c.122G>T MANE Select NP_002973.1:p.Arg41Met
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