Canonical Allele Identifier: CA2597831007
Gene: SLC22A8 HGNC NCBI

Linked Data

dbSNP Id: rs2135110224

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991108_62991110del , CM000673.2:g.62991108_62991110del GRCh38
NC_000011.9:g.62758580_62758582del , CM000673.1:g.62758580_62758582del GRCh37
NC_000011.8:g.62515156_62515158del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000539841.1:n.5628_5630del