Canonical Allele Identifier: CA2256959552
Gene: CCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255373G= , CM000679.2:g.34255373G= GRCh38
NC_000017.10:g.32582392G= , CM000679.1:g.32582392G= GRCh37
NC_000017.9:g.29606505G= NCBI36
NG_012123.1:g.5097G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.24G= ENSP00000462156.1:p.Leu8=
ENST00000624362.2:n.89G=
ENST00000225831.4:c.24G= MANE Select ENSP00000225831.4:p.Leu8=
ENST00000580907.5:c.24G= ENSP00000462156.1:p.Leu8=
ENST00000624362.1:n.156G=
NM_002982.3:c.24G= NP_002973.1:p.Leu8=
NM_002982.4:c.24G= MANE Select NP_002973.1:p.Leu8=