Canonical Allele Identifier: CA2614031332
Gene: SLC22A8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991303G>A , CM000673.2:g.62991303G>A GRCh38
NC_000011.9:g.62758775G>A , CM000673.1:g.62758775G>A GRCh37
NC_000011.8:g.62515351G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000539841.1:n.5429C>T