Canonical Allele Identifier: CA2724468289
Gene: SLC22A8 HGNC NCBI

Linked Data

dbSNP Id: rs2135110292
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991221T>G , CM000673.2:g.62991221T>G GRCh38
NC_000011.9:g.62758693T>G , CM000673.1:g.62758693T>G GRCh37
NC_000011.8:g.62515269T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000539841.1:n.5511A>C
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