Canonical Allele Identifier: CA399059782
Gene: CCL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255408A>T , CM000679.2:g.34255408A>T GRCh38
NC_000017.10:g.32582427A>T , CM000679.1:g.32582427A>T GRCh37
NC_000017.9:g.29606540A>T NCBI36
NG_012123.1:g.5132A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.59A>T ENSP00000462156.1:p.Gln20Leu
ENST00000624362.2:n.124A>T
ENST00000225831.4:c.59A>T MANE Select ENSP00000225831.4:p.Gln20Leu
ENST00000580907.5:c.59A>T ENSP00000462156.1:p.Gln20Leu
ENST00000624362.1:n.191A>T
NM_002982.3:c.59A>T NP_002973.1:p.Gln20Leu
NM_002982.4:c.59A>T MANE Select NP_002973.1:p.Gln20Leu