Canonical Allele Identifier: CA2637213917
Gene: CCL8 HGNC NCBI

Linked Data

gnomAD v4: 17-34320720-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34320720T>G , CM000679.2:g.34320720T>G GRCh38
NC_000017.10:g.32647739T>G , CM000679.1:g.32647739T>G GRCh37
NC_000017.9:g.29671852T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000394620.2:c.195-82T>G MANE Select ENSP00000378118.1:n.195-82T>G
ENST00000394620.1:c.195-82T>G ENSP00000378118.1:n.195-82T>G
NM_005623.2:c.195-82T>G NP_005614.2:n.195-82T>G
NM_005623.3:c.195-82T>G MANE Select NP_005614.2:n.195-82T>G
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