Canonical Allele Identifier: CA2637213906
Gene: CCL8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34320712del , CM000679.2:g.34320712del GRCh38
NC_000017.10:g.32647731del , CM000679.1:g.32647731del GRCh37
NC_000017.9:g.29671844del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000394620.2:c.195-90del MANE Select ENSP00000378118.1:n.195-90del
ENST00000394620.1:c.195-90del ENSP00000378118.1:n.195-90del
NM_005623.2:c.195-90del NP_005614.2:n.195-90del
NM_005623.3:c.195-90del MANE Select NP_005614.2:n.195-90del