Canonical Allele Identifier: CA2256994439
Gene: CCL8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34320734C= , CM000679.2:g.34320734C= GRCh38
NC_000017.10:g.32647753C= , CM000679.1:g.32647753C= GRCh37
NC_000017.9:g.29671866C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000394620.2:c.195-68C= MANE Select ENSP00000378118.1:n.195-68C=
ENST00000394620.1:c.195-68C= ENSP00000378118.1:n.195-68C=
NM_005623.2:c.195-68C= NP_005614.2:n.195-68C=
NM_005623.3:c.195-68C= MANE Select NP_005614.2:n.195-68C=