Canonical Allele Identifier: CA679091803

Gene: SLC22A8

Linked Data

• dbSNP Id: rs1169425646
• gnomAD v3: 11-62991195-A-G
• gnomAD v4: 11-62991195-A-G
• MyVariant Identifiers: chr11:g.62758667A>G (hg19) ; chr11:g.62991195A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62991195A>G , CM000673.2:g.62991195A>G	GRCh38
NC_000011.9:g.62758667A>G , CM000673.1:g.62758667A>G	GRCh37
NC_000011.8:g.62515243A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539841.1:n.5537T>C