Canonical Allele Identifier: CA2724234976
Gene: SLC22A8 HGNC NCBI

Linked Data

dbSNP Id: rs1361002273
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991159C>T , CM000673.2:g.62991159C>T GRCh38
NC_000011.9:g.62758631C>T , CM000673.1:g.62758631C>T GRCh37
NC_000011.8:g.62515207C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000539841.1:n.5573G>A
Search 100 bp 5'
Search 100 bp 3'