ClinGen Allele Registry
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Canonical Allele Identifier:
CA13462152
Gene: SLC22A8
HGNC
NCBI
Linked Data
dbSNP Id:
rs10792367
gnomAD v2:
11-62758799-C-G
gnomAD v3:
11-62991327-C-G
gnomAD v4:
11-62991327-C-G
MyVariant Identifiers:
chr11:g.62758799C>G (hg19)
chr11:g.62991327C>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.62991327C>G , CM000673.2:g.62991327C>G
GRCh38
NC_000011.9:g.62758799C>G , CM000673.1:g.62758799C>G
GRCh37
NC_000011.8:g.62515375C>G
NCBI36
Transcript Alleles
HGVS
Amino-acid change
ENST00000539841.1:n.5405G>C
Search 100 bp 5'
Search 100 bp 3'