Canonical Allele Identifier: CA2256959980
Gene: CCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256314A= , CM000679.2:g.34256314A= GRCh38
NC_000017.10:g.32583333A= , CM000679.1:g.32583333A= GRCh37
NC_000017.9:g.29607446A= NCBI36
NG_012123.1:g.6038A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.169A= ENSP00000462156.1:p.Ser57=
ENST00000624362.2:n.1030A=
ENST00000225831.4:c.169A= MANE Select ENSP00000225831.4:p.Ser57=
ENST00000580907.5:c.169A= ENSP00000462156.1:p.Ser57=
ENST00000582017.1:n.107A=
NM_002982.3:c.169A= NP_002973.1:p.Ser57=
NM_002982.4:c.169A= MANE Select NP_002973.1:p.Ser57=