Canonical Allele Identifier: CA399060145
Gene: CCL2 HGNC NCBI

Linked Data

COSMIC: COSM5820054
MyVariant Identifiers: chr17:g.32583318A>T (hg19) chr17:g.34256299A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256299A>T , CM000679.2:g.34256299A>T GRCh38
NC_000017.10:g.32583318A>T , CM000679.1:g.32583318A>T GRCh37
NC_000017.9:g.29607431A>T NCBI36
NG_012123.1:g.6023A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.154A>T ENSP00000462156.1:p.Arg52Ter
ENST00000624362.2:n.1015A>T
ENST00000225831.4:c.154A>T MANE Select ENSP00000225831.4:p.Arg52Ter
ENST00000580907.5:c.154A>T ENSP00000462156.1:p.Arg52Ter
ENST00000582017.1:n.92A>T
NM_002982.3:c.154A>T NP_002973.1:p.Arg52Ter
NM_002982.4:c.154A>T MANE Select NP_002973.1:p.Arg52Ter
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