Canonical Allele Identifier: CA399060002
Gene: CCL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256259C>A , CM000679.2:g.34256259C>A GRCh38
NC_000017.10:g.32583278C>A , CM000679.1:g.32583278C>A GRCh37
NC_000017.9:g.29607391C>A NCBI36
NG_012123.1:g.5983C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000580907.6:c.114C>A ENSP00000462156.1:p.Phe38Leu
ENST00000624362.2:n.975C>A
ENST00000225831.4:c.114C>A MANE Select ENSP00000225831.4:p.Phe38Leu
ENST00000580907.5:c.114C>A ENSP00000462156.1:p.Phe38Leu
ENST00000582017.1:n.52C>A
NM_002982.3:c.114C>A NP_002973.1:p.Phe38Leu
NM_002982.4:c.114C>A MANE Select NP_002973.1:p.Phe38Leu