Canonical Allele Identifier: CA2637213909
Gene: CCL8 HGNC NCBI

Linked Data

gnomAD v4: 17-34320714-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34320714G>A , CM000679.2:g.34320714G>A GRCh38
NC_000017.10:g.32647733G>A , CM000679.1:g.32647733G>A GRCh37
NC_000017.9:g.29671846G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000394620.2:c.195-88G>A MANE Select ENSP00000378118.1:n.195-88G>A
ENST00000394620.1:c.195-88G>A ENSP00000378118.1:n.195-88G>A
NM_005623.2:c.195-88G>A NP_005614.2:n.195-88G>A
NM_005623.3:c.195-88G>A MANE Select NP_005614.2:n.195-88G>A
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