ClinGen Allele Registry
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Canonical Allele Identifier:
CA679091839
Gene: SLC22A8
HGNC
NCBI
Linked Data
dbSNP Id:
rs1437150393
gnomAD v3:
11-62991318-T-C
gnomAD v4:
11-62991318-T-C
MyVariant Identifiers:
chr11:g.62758790T>C (hg19)
chr11:g.62991318T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.62991318T>C , CM000673.2:g.62991318T>C
GRCh38
NC_000011.9:g.62758790T>C , CM000673.1:g.62758790T>C
GRCh37
NC_000011.8:g.62515366T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000539841.1:n.5414A>G
Search 100 bp 5'
Search 100 bp 3'