Canonical Allele Identifier: CA2614031331
Gene: SLC22A8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991297G>T , CM000673.2:g.62991297G>T GRCh38
NC_000011.9:g.62758769G>T , CM000673.1:g.62758769G>T GRCh37
NC_000011.8:g.62515345G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000539841.1:n.5435C>A