Canonical Allele Identifier: CA223621079
Gene: SLC22A8 HGNC NCBI

Linked Data

dbSNP Id: rs950737713
MyVariant Identifiers: chr11:g.62991342G>A (hg38)

Genomic Alleles

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

Transcript Alleles

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