Canonical Allele Identifier: CA2256994434
Gene: CCL8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34320725T= , CM000679.2:g.34320725T= GRCh38
NC_000017.10:g.32647744T= , CM000679.1:g.32647744T= GRCh37
NC_000017.9:g.29671857T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000394620.2:c.195-77T= MANE Select ENSP00000378118.1:n.195-77T=
ENST00000394620.1:c.195-77T= ENSP00000378118.1:n.195-77T=
NM_005623.2:c.195-77T= NP_005614.2:n.195-77T=
NM_005623.3:c.195-77T= MANE Select NP_005614.2:n.195-77T=