Canonical Allele Identifier: CA1978008812
Gene: SLC22A8 HGNC NCBI

Linked Data

dbSNP Id: rs2086346893

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991253A>C , CM000673.2:g.62991253A>C GRCh38
NC_000011.9:g.62758725A>C , CM000673.1:g.62758725A>C GRCh37
NC_000011.8:g.62515301A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000539841.1:n.5479T>G