Canonical Allele Identifier: CA399060064
Gene: CCL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256273T>A , CM000679.2:g.34256273T>A GRCh38
NC_000017.10:g.32583292T>A , CM000679.1:g.32583292T>A GRCh37
NC_000017.9:g.29607405T>A NCBI36
NG_012123.1:g.5997T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.128T>A ENSP00000462156.1:p.Ile43Asn
ENST00000624362.2:n.989T>A
ENST00000225831.4:c.128T>A MANE Select ENSP00000225831.4:p.Ile43Asn
ENST00000580907.5:c.128T>A ENSP00000462156.1:p.Ile43Asn
ENST00000582017.1:n.66T>A
NM_002982.3:c.128T>A NP_002973.1:p.Ile43Asn
NM_002982.4:c.128T>A MANE Select NP_002973.1:p.Ile43Asn