Canonical Allele Identifier: CA2520531821
Gene: SLC22A8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991136T>A , CM000673.2:g.62991136T>A GRCh38
NC_000011.9:g.62758608T>A , CM000673.1:g.62758608T>A GRCh37
NC_000011.8:g.62515184T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000539841.1:n.5596A>T
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