Canonical Allele Identifier: CA8495430
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs565820582

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256195G>T , CM000679.2:g.34256195G>T GRCh38
NC_000017.10:g.32583214G>T , CM000679.1:g.32583214G>T GRCh37
NC_000017.9:g.29607327G>T NCBI36
NG_012123.1:g.5919G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.77-27G>T ENSP00000462156.1:n.77-27G>T
ENST00000624362.2:n.911G>T
ENST00000225831.4:c.77-27G>T MANE Select ENSP00000225831.4:n.77-27G>T
ENST00000580907.5:c.77-27G>T ENSP00000462156.1:n.77-27G>T
ENST00000624362.1:n.978G>T
NM_002982.3:c.77-27G>T NP_002973.1:n.77-27G>T
NM_002982.4:c.77-27G>T MANE Select NP_002973.1:n.77-27G>T