Canonical Allele Identifier: CA679091858
Gene: SLC22A8 HGNC NCBI

Linked Data

dbSNP Id: rs950737713

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991342G>T , CM000673.2:g.62991342G>T GRCh38
NC_000011.9:g.62758814G>T , CM000673.1:g.62758814G>T GRCh37
NC_000011.8:g.62515390G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000539841.1:n.5390C>A