Canonical Allele Identifier: CA2256960003
Gene: CCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256377C= , CM000679.2:g.34256377C= GRCh38
NC_000017.10:g.32583396C= , CM000679.1:g.32583396C= GRCh37
NC_000017.9:g.29607509C= NCBI36
NG_012123.1:g.6101C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.*34C= ENSP00000462156.1:n.*34C=
ENST00000624362.2:n.1093C=
ENST00000225831.4:c.194+38C= MANE Select ENSP00000225831.4:n.194+38C=
ENST00000580907.5:c.*34C= ENSP00000462156.1:n.*34C=
ENST00000582017.1:n.170C=
NM_002982.3:c.194+38C= NP_002973.1:n.194+38C=
NM_002982.4:c.194+38C= MANE Select NP_002973.1:n.194+38C=