Canonical Allele Identifier: CA599569053

Gene: SLC22A8

Linked Data

• dbSNP Id: rs1454145594
• gnomAD v2: 11-62758730-C-G
• gnomAD v3: 11-62991258-C-G
• gnomAD v4: 11-62991258-C-G
• MyVariant Identifiers: chr11:g.62758730C>G (hg19) ; chr11:g.62991258C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62991258C>G , CM000673.2:g.62991258C>G	GRCh38
NC_000011.9:g.62758730C>G , CM000673.1:g.62758730C>G	GRCh37
NC_000011.8:g.62515306C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539841.1:n.5474G>C