Canonical Allele Identifier: CA2256959959
Gene: CCL2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.122G= ENSP00000462156.1:p.Arg41=
ENST00000624362.2:n.983G=
ENST00000225831.4:c.122G= MANE Select ENSP00000225831.4:p.Arg41=
ENST00000580907.5:c.122G= ENSP00000462156.1:p.Arg41=
ENST00000582017.1:n.60G=
NM_002982.3:c.122G= NP_002973.1:p.Arg41=
NM_002982.4:c.122G= MANE Select NP_002973.1:p.Arg41=