Canonical Allele Identifier: CA679091845
Gene: SLC22A8 HGNC NCBI

Linked Data

dbSNP Id: rs1166574178
MyVariant Identifiers: chr11:g.62758796G>A (hg19) chr11:g.62991324G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991324G>A , CM000673.2:g.62991324G>A GRCh38
NC_000011.9:g.62758796G>A , CM000673.1:g.62758796G>A GRCh37
NC_000011.8:g.62515372G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000539841.1:n.5408C>T
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