Canonical Allele Identifier: CA2614031344
Gene: SLC22A8 HGNC NCBI

Linked Data

gnomAD v4: 11-62991328-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991328T>C , CM000673.2:g.62991328T>C GRCh38
NC_000011.9:g.62758800T>C , CM000673.1:g.62758800T>C GRCh37
NC_000011.8:g.62515376T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000539841.1:n.5404A>G
Search 100 bp 5'
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