Canonical Allele Identifier: CA2576229867
Gene: CCL8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34320722A>T , CM000679.2:g.34320722A>T GRCh38
NC_000017.10:g.32647741A>T , CM000679.1:g.32647741A>T GRCh37
NC_000017.9:g.29671854A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000394620.2:c.195-80A>T MANE Select ENSP00000378118.1:n.195-80A>T
ENST00000394620.1:c.195-80A>T ENSP00000378118.1:n.195-80A>T
NM_005623.2:c.195-80A>T NP_005614.2:n.195-80A>T
NM_005623.3:c.195-80A>T MANE Select NP_005614.2:n.195-80A>T