Canonical Allele Identifier: CA2637210692
Gene: CCL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256384_34256385insC , CM000679.2:g.34256384_34256385insC GRCh38
NC_000017.10:g.32583403_32583404insC , CM000679.1:g.32583403_32583404insC GRCh37
NC_000017.9:g.29607516_29607517insC NCBI36
NG_012123.1:g.6108_6109insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.*41_*42insC ENSP00000462156.1:n.*41_*42insC
ENST00000624362.2:n.1100_1101insC
ENST00000225831.4:c.194+45_194+46insC MANE Select ENSP00000225831.4:n.194+45_194+46insC
ENST00000580907.5:c.*41_*42insC ENSP00000462156.1:n.*41_*42insC
ENST00000582017.1:n.177_178insC
NM_002982.3:c.194+45_194+46insC NP_002973.1:n.194+45_194+46insC
NM_002982.4:c.194+45_194+46insC MANE Select NP_002973.1:n.194+45_194+46insC