Canonical Allele Identifier: CA938740770

Gene: SLC22A8

Linked Data

• dbSNP Id: rs1310130913
• gnomAD v3: 11-62991305-G-C
• gnomAD v4: 11-62991305-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62991305G>C , CM000673.2:g.62991305G>C	GRCh38
NC_000011.9:g.62758777G>C , CM000673.1:g.62758777G>C	GRCh37
NC_000011.8:g.62515353G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539841.1:n.5427C>G