Canonical Allele Identifier: CA679091774
Gene: SLC22A8 HGNC NCBI

Linked Data

dbSNP Id: rs1244788970

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991111_62991115del , CM000673.2:g.62991111_62991115del GRCh38
NC_000011.9:g.62758583_62758587del , CM000673.1:g.62758583_62758587del GRCh37
NC_000011.8:g.62515159_62515163del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000539841.1:n.5623_5627del