Canonical Allele Identifier: CA656589001
Gene: CCL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256538T>G , CM000679.2:g.34256538T>G GRCh38
NC_000017.10:g.32583557T>G , CM000679.1:g.32583557T>G GRCh37
NC_000017.9:g.29607670T>G NCBI36
NG_012123.1:g.6262T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.*195T>G ENSP00000462156.1:n.*195T>G
ENST00000624362.2:n.1254T>G
ENST00000225831.4:c.195-184T>G MANE Select ENSP00000225831.4:n.195-184T>G
ENST00000580907.5:c.*195T>G ENSP00000462156.1:n.*195T>G
ENST00000582017.1:n.331T>G
NM_002982.3:c.195-184T>G NP_002973.1:n.195-184T>G
NM_002982.4:c.195-184T>G MANE Select NP_002973.1:n.195-184T>G