Canonical Allele Identifier: CA2256960000
Gene: CCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256367G= , CM000679.2:g.34256367G= GRCh38
NC_000017.10:g.32583386G= , CM000679.1:g.32583386G= GRCh37
NC_000017.9:g.29607499G= NCBI36
NG_012123.1:g.6091G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.*24G= ENSP00000462156.1:n.*24G=
ENST00000624362.2:n.1083G=
ENST00000225831.4:c.194+28G= MANE Select ENSP00000225831.4:n.194+28G=
ENST00000580907.5:c.*24G= ENSP00000462156.1:n.*24G=
ENST00000582017.1:n.160G=
NM_002982.3:c.194+28G= NP_002973.1:n.194+28G=
NM_002982.4:c.194+28G= MANE Select NP_002973.1:n.194+28G=