Canonical Allele Identifier: CA8495410
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs778276611

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255396C>G , CM000679.2:g.34255396C>G GRCh38
NC_000017.10:g.32582415C>G , CM000679.1:g.32582415C>G GRCh37
NC_000017.9:g.29606528C>G NCBI36
NG_012123.1:g.5120C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.47C>G ENSP00000462156.1:p.Thr16Ser
ENST00000624362.2:n.112C>G
ENST00000225831.4:c.47C>G MANE Select ENSP00000225831.4:p.Thr16Ser
ENST00000580907.5:c.47C>G ENSP00000462156.1:p.Thr16Ser
ENST00000624362.1:n.179C>G
NM_002982.3:c.47C>G NP_002973.1:p.Thr16Ser
NM_002982.4:c.47C>G MANE Select NP_002973.1:p.Thr16Ser