Canonical Allele Identifier: CA2256959930
Gene: CCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256188C= , CM000679.2:g.34256188C= GRCh38
NC_000017.10:g.32583207C= , CM000679.1:g.32583207C= GRCh37
NC_000017.9:g.29607320C= NCBI36
NG_012123.1:g.5912C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.77-34C= ENSP00000462156.1:n.77-34C=
ENST00000624362.2:n.904C=
ENST00000225831.4:c.77-34C= MANE Select ENSP00000225831.4:n.77-34C=
ENST00000580907.5:c.77-34C= ENSP00000462156.1:n.77-34C=
ENST00000624362.1:n.971C=
NM_002982.3:c.77-34C= NP_002973.1:n.77-34C=
NM_002982.4:c.77-34C= MANE Select NP_002973.1:n.77-34C=