Canonical Allele Identifier: CA2637213907
Gene: CCL8 HGNC NCBI

Linked Data

gnomAD v4: 17-34320712-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34320712A>T , CM000679.2:g.34320712A>T GRCh38
NC_000017.10:g.32647731A>T , CM000679.1:g.32647731A>T GRCh37
NC_000017.9:g.29671844A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000394620.2:c.195-90A>T MANE Select ENSP00000378118.1:n.195-90A>T
ENST00000394620.1:c.195-90A>T ENSP00000378118.1:n.195-90A>T
NM_005623.2:c.195-90A>T NP_005614.2:n.195-90A>T
NM_005623.3:c.195-90A>T MANE Select NP_005614.2:n.195-90A>T
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