Canonical Allele Identifier: CA399059808
Gene: CCL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255421G>T , CM000679.2:g.34255421G>T GRCh38
NC_000017.10:g.32582440G>T , CM000679.1:g.32582440G>T GRCh37
NC_000017.9:g.29606553G>T NCBI36
NG_012123.1:g.5145G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.72G>T ENSP00000462156.1:p.Gln24His
ENST00000624362.2:n.137G>T
ENST00000225831.4:c.72G>T MANE Select ENSP00000225831.4:p.Gln24His
ENST00000580907.5:c.72G>T ENSP00000462156.1:p.Gln24His
ENST00000624362.1:n.204G>T
NM_002982.3:c.72G>T NP_002973.1:p.Gln24His
NM_002982.4:c.72G>T MANE Select NP_002973.1:p.Gln24His