Canonical Allele Identifier: CA679091839
Gene: SLC22A8 HGNC NCBI

Linked Data

dbSNP Id: rs1437150393

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991318T>C , CM000673.2:g.62991318T>C GRCh38
NC_000011.9:g.62758790T>C , CM000673.1:g.62758790T>C GRCh37
NC_000011.8:g.62515366T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000539841.1:n.5414A>G