Canonical Allele Identifier: CA625524307
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs1445576477

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256193A>G , CM000679.2:g.34256193A>G GRCh38
NC_000017.10:g.32583212A>G , CM000679.1:g.32583212A>G GRCh37
NC_000017.9:g.29607325A>G NCBI36
NG_012123.1:g.5917A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.77-29A>G ENSP00000462156.1:n.77-29A>G
ENST00000624362.2:n.909A>G
ENST00000225831.4:c.77-29A>G MANE Select ENSP00000225831.4:n.77-29A>G
ENST00000580907.5:c.77-29A>G ENSP00000462156.1:n.77-29A>G
ENST00000624362.1:n.976A>G
NM_002982.3:c.77-29A>G NP_002973.1:n.77-29A>G
NM_002982.4:c.77-29A>G MANE Select NP_002973.1:n.77-29A>G