Canonical Allele Identifier: CA2256960014
Gene: CCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256395G= , CM000679.2:g.34256395G= GRCh38
NC_000017.10:g.32583414G= , CM000679.1:g.32583414G= GRCh37
NC_000017.9:g.29607527G= NCBI36
NG_012123.1:g.6119G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.*52G= ENSP00000462156.1:n.*52G=
ENST00000624362.2:n.1111G=
ENST00000225831.4:c.194+56G= MANE Select ENSP00000225831.4:n.194+56G=
ENST00000580907.5:c.*52G= ENSP00000462156.1:n.*52G=
ENST00000582017.1:n.188G=
NM_002982.3:c.194+56G= NP_002973.1:n.194+56G=
NM_002982.4:c.194+56G= MANE Select NP_002973.1:n.194+56G=