Canonical Allele Identifier: CA2637210707
Gene: CCL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256413A>G , CM000679.2:g.34256413A>G GRCh38
NC_000017.10:g.32583432A>G , CM000679.1:g.32583432A>G GRCh37
NC_000017.9:g.29607545A>G NCBI36
NG_012123.1:g.6137A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.*70A>G ENSP00000462156.1:n.*70A>G
ENST00000624362.2:n.1129A>G
ENST00000225831.4:c.194+74A>G MANE Select ENSP00000225831.4:n.194+74A>G
ENST00000580907.5:c.*70A>G ENSP00000462156.1:n.*70A>G
ENST00000582017.1:n.206A>G
NM_002982.3:c.194+74A>G NP_002973.1:n.194+74A>G
NM_002982.4:c.194+74A>G MANE Select NP_002973.1:n.194+74A>G