Canonical Allele Identifier: CA599569052

Gene: SLC22A8

Linked Data

• dbSNP Id: rs1489105445
• gnomAD v2: 11-62758704-G-C
• MyVariant Identifiers: chr11:g.62758704G>C (hg19) ; chr11:g.62991232G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62991232G>C , CM000673.2:g.62991232G>C	GRCh38
NC_000011.9:g.62758704G>C , CM000673.1:g.62758704G>C	GRCh37
NC_000011.8:g.62515280G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539841.1:n.5500C>G