Canonical Allele Identifier: CA2256959828
Gene: CCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255957_34255958delinsTG , CM000679.2:g.34255957_34255958delinsTG GRCh38
NC_000017.10:g.32582976_32582977delinsTG , CM000679.1:g.32582976_32582977delinsTG GRCh37
NC_000017.9:g.29607089_29607090delinsTG NCBI36
NG_012123.1:g.5681_5682delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.77-265_77-264delinsTG ENSP00000462156.1:n.77-265_77-264delinsTG
ENST00000624362.2:n.673_674delinsTG
ENST00000225831.4:c.77-265_77-264delinsTG MANE Select ENSP00000225831.4:n.77-265_77-264delinsTG
ENST00000580907.5:c.77-265_77-264delinsTG ENSP00000462156.1:n.77-265_77-264delinsTG
ENST00000624362.1:n.740_741delinsTG
NM_002982.3:c.77-265_77-264delinsTG NP_002973.1:n.77-265_77-264delinsTG
NM_002982.4:c.77-265_77-264delinsTG MANE Select NP_002973.1:n.77-265_77-264delinsTG