Canonical Allele Identifier: CA399059758
Gene: CCL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255398T>C , CM000679.2:g.34255398T>C GRCh38
NC_000017.10:g.32582417T>C , CM000679.1:g.32582417T>C GRCh37
NC_000017.9:g.29606530T>C NCBI36
NG_012123.1:g.5122T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.49T>C ENSP00000462156.1:p.Phe17Leu
ENST00000624362.2:n.114T>C
ENST00000225831.4:c.49T>C MANE Select ENSP00000225831.4:p.Phe17Leu
ENST00000580907.5:c.49T>C ENSP00000462156.1:p.Phe17Leu
ENST00000624362.1:n.181T>C
NM_002982.3:c.49T>C NP_002973.1:p.Phe17Leu
NM_002982.4:c.49T>C MANE Select NP_002973.1:p.Phe17Leu