Canonical Allele Identifier: CA1978008821
Gene: SLC22A8 HGNC NCBI

Linked Data

dbSNP Id: rs2086346959

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991265A>G , CM000673.2:g.62991265A>G GRCh38
NC_000011.9:g.62758737A>G , CM000673.1:g.62758737A>G GRCh37
NC_000011.8:g.62515313A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000539841.1:n.5467T>C