Canonical Allele Identifier: CA1978008892
Gene: SLC22A8 HGNC NCBI

Linked Data

dbSNP Id: rs2086347566

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991359C>T , CM000673.2:g.62991359C>T GRCh38
NC_000011.9:g.62758831C>T , CM000673.1:g.62758831C>T GRCh37
NC_000011.8:g.62515407C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000539841.1:n.5373G>A