Canonical Allele Identifier: CA2256959937
Gene: CCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256201T= , CM000679.2:g.34256201T= GRCh38
NC_000017.10:g.32583220T= , CM000679.1:g.32583220T= GRCh37
NC_000017.9:g.29607333T= NCBI36
NG_012123.1:g.5925T=

Transcript Alleles

HGVS Amino-acid change
ENST00000580907.6:c.77-21T= ENSP00000462156.1:n.77-21T=
ENST00000624362.2:n.917T=
ENST00000225831.4:c.77-21T= MANE Select ENSP00000225831.4:n.77-21T=
ENST00000580907.5:c.77-21T= ENSP00000462156.1:n.77-21T=
ENST00000624362.1:n.984T=
NM_002982.3:c.77-21T= NP_002973.1:n.77-21T=
NM_002982.4:c.77-21T= MANE Select NP_002973.1:n.77-21T=