Canonical Allele Identifier: CA2256994427
Gene: CCL8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34320713G= , CM000679.2:g.34320713G= GRCh38
NC_000017.10:g.32647732G= , CM000679.1:g.32647732G= GRCh37
NC_000017.9:g.29671845G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000394620.2:c.195-89G= MANE Select ENSP00000378118.1:n.195-89G=
ENST00000394620.1:c.195-89G= ENSP00000378118.1:n.195-89G=
NM_005623.2:c.195-89G= NP_005614.2:n.195-89G=
NM_005623.3:c.195-89G= MANE Select NP_005614.2:n.195-89G=