Canonical Allele Identifier: CA679091799

Gene: SLC22A8

Linked Data

• dbSNP Id: rs1422714711
• MyVariant Identifiers: chr11:g.62758666C>T (hg19) ; chr11:g.62991194C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62991194C>T , CM000673.2:g.62991194C>T	GRCh38
NC_000011.9:g.62758666C>T , CM000673.1:g.62758666C>T	GRCh37
NC_000011.8:g.62515242C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539841.1:n.5538G>A