Canonical Allele Identifier: CA2637213922
Gene: CCL8 HGNC NCBI

Linked Data

gnomAD v4: 17-34320726-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34320726C>A , CM000679.2:g.34320726C>A GRCh38
NC_000017.10:g.32647745C>A , CM000679.1:g.32647745C>A GRCh37
NC_000017.9:g.29671858C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000394620.2:c.195-76C>A MANE Select ENSP00000378118.1:n.195-76C>A
ENST00000394620.1:c.195-76C>A ENSP00000378118.1:n.195-76C>A
NM_005623.2:c.195-76C>A NP_005614.2:n.195-76C>A
NM_005623.3:c.195-76C>A MANE Select NP_005614.2:n.195-76C>A
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