Canonical Allele Identifier: CA2581303071
Gene: CCL8 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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