Canonical Allele Identifier: CA2724468290
Gene: SLC22A8 HGNC NCBI

Linked Data

dbSNP Id: rs2135110386

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991376A>G , CM000673.2:g.62991376A>G GRCh38
NC_000011.9:g.62758848A>G , CM000673.1:g.62758848A>G GRCh37
NC_000011.8:g.62515424A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000539841.1:n.5356T>C