Canonical Allele Identifier: CA2614031362

Gene: SLC22A8

Linked Data

• gnomAD v4: 11-62991395-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62991395G>T , CM000673.2:g.62991395G>T	GRCh38
NC_000011.9:g.62758867G>T , CM000673.1:g.62758867G>T	GRCh37
NC_000011.8:g.62515443G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539841.1:n.5337C>A