Canonical Allele Identifier: CA2256960001
Gene: CCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256372A= , CM000679.2:g.34256372A= GRCh38
NC_000017.10:g.32583391A= , CM000679.1:g.32583391A= GRCh37
NC_000017.9:g.29607504A= NCBI36
NG_012123.1:g.6096A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.*29A= ENSP00000462156.1:n.*29A=
ENST00000624362.2:n.1088A=
ENST00000225831.4:c.194+33A= MANE Select ENSP00000225831.4:n.194+33A=
ENST00000580907.5:c.*29A= ENSP00000462156.1:n.*29A=
ENST00000582017.1:n.165A=
NM_002982.3:c.194+33A= NP_002973.1:n.194+33A=
NM_002982.4:c.194+33A= MANE Select NP_002973.1:n.194+33A=