Canonical Allele Identifier: CA223621057
Gene: SLC22A8 HGNC NCBI

Linked Data

dbSNP Id: rs545100939
MyVariant Identifiers: chr11:g.62991304C>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991304C>A , CM000673.2:g.62991304C>A GRCh38
NC_000011.9:g.62758776C>A , CM000673.1:g.62758776C>A GRCh37
NC_000011.8:g.62515352C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000539841.1:n.5428G>T