Canonical Allele Identifier: CA679091789

Gene: SLC22A8

Linked Data

• dbSNP Id: rs1366545020
• gnomAD v3: 11-62991147-GTTTTC-G
• gnomAD v4: 11-62991147-GTTTTC-G
• MyVariant Identifiers: chr11:g.62758620_62758624del (hg19) ; chr11:g.62991148_62991152del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62991152_62991156del , CM000673.2:g.62991152_62991156del	GRCh38
NC_000011.9:g.62758624_62758628del , CM000673.1:g.62758624_62758628del	GRCh37
NC_000011.8:g.62515200_62515204del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539841.1:n.5580_5584del