Canonical Allele Identifier: CA13462152
Gene: SLC22A8 HGNC NCBI

Linked Data

dbSNP Id: rs10792367

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991327C>G , CM000673.2:g.62991327C>G GRCh38
NC_000011.9:g.62758799C>G , CM000673.1:g.62758799C>G GRCh37
NC_000011.8:g.62515375C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000539841.1:n.5405G>C