Canonical Allele Identifier: CA679091861
Gene: SLC22A8 HGNC NCBI

Linked Data

dbSNP Id: rs1483560453

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991353A>G , CM000673.2:g.62991353A>G GRCh38
NC_000011.9:g.62758825A>G , CM000673.1:g.62758825A>G GRCh37
NC_000011.8:g.62515401A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000539841.1:n.5379T>C