ClinGen Allele Registry
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Canonical Allele Identifier:
CA679091832
Gene: SLC22A8
HGNC
NCBI
Linked Data
dbSNP Id:
rs1447476846
gnomAD v3:
11-62991302-A-G
gnomAD v4:
11-62991302-A-G
MyVariant Identifiers:
chr11:g.62758774A>G (hg19)
chr11:g.62991302A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.62991302A>G , CM000673.2:g.62991302A>G
GRCh38
NC_000011.9:g.62758774A>G , CM000673.1:g.62758774A>G
GRCh37
NC_000011.8:g.62515350A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000539841.1:n.5430T>C
Search 100 bp 5'
Search 100 bp 3'