Canonical Allele Identifier: CA2256959998
Gene: CCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256365T= , CM000679.2:g.34256365T= GRCh38
NC_000017.10:g.32583384T= , CM000679.1:g.32583384T= GRCh37
NC_000017.9:g.29607497T= NCBI36
NG_012123.1:g.6089T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.*22T= ENSP00000462156.1:n.*22T=
ENST00000624362.2:n.1081T=
ENST00000225831.4:c.194+26T= MANE Select ENSP00000225831.4:n.194+26T=
ENST00000580907.5:c.*22T= ENSP00000462156.1:n.*22T=
ENST00000582017.1:n.158T=
NM_002982.3:c.194+26T= NP_002973.1:n.194+26T=
NM_002982.4:c.194+26T= MANE Select NP_002973.1:n.194+26T=