Canonical Allele Identifier: CA1978008901
Gene: SLC22A8 HGNC NCBI

Linked Data

dbSNP Id: rs2086347610

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991371G>A , CM000673.2:g.62991371G>A GRCh38
NC_000011.9:g.62758843G>A , CM000673.1:g.62758843G>A GRCh37
NC_000011.8:g.62515419G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000539841.1:n.5361C>T