Canonical Allele Identifier: CA2637210443
Gene: CCL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255977_34255978del , CM000679.2:g.34255977_34255978del GRCh38
NC_000017.10:g.32582996_32582997del , CM000679.1:g.32582996_32582997del GRCh37
NC_000017.9:g.29607109_29607110del NCBI36
NG_012123.1:g.5701_5702del

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.77-245_77-244del ENSP00000462156.1:n.77-245_77-244del
ENST00000624362.2:n.693_694del
ENST00000225831.4:c.77-245_77-244del MANE Select ENSP00000225831.4:n.77-245_77-244del
ENST00000580907.5:c.77-245_77-244del ENSP00000462156.1:n.77-245_77-244del
ENST00000624362.1:n.760_761del
NM_002982.3:c.77-245_77-244del NP_002973.1:n.77-245_77-244del
NM_002982.4:c.77-245_77-244del MANE Select NP_002973.1:n.77-245_77-244del