Canonical Allele Identifier: CA2256994435
Gene: CCL8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34320727T= , CM000679.2:g.34320727T= GRCh38
NC_000017.10:g.32647746T= , CM000679.1:g.32647746T= GRCh37
NC_000017.9:g.29671859T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000394620.2:c.195-75T= MANE Select ENSP00000378118.1:n.195-75T=
ENST00000394620.1:c.195-75T= ENSP00000378118.1:n.195-75T=
NM_005623.2:c.195-75T= NP_005614.2:n.195-75T=
NM_005623.3:c.195-75T= MANE Select NP_005614.2:n.195-75T=
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