Canonical Allele Identifier: CA938740785

Gene: SLC22A8

Linked Data

• dbSNP Id: rs2086347670
• gnomAD v3: 11-62991380-A-C
• gnomAD v4: 11-62991380-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62991380A>C , CM000673.2:g.62991380A>C	GRCh38
NC_000011.9:g.62758852A>C , CM000673.1:g.62758852A>C	GRCh37
NC_000011.8:g.62515428A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539841.1:n.5352T>G