ClinGen Allele Registry
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Canonical Allele Identifier:
CA12732213
Gene: OTUD6B-AS1
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.91063415A>C
GRCh37
chr8:g.92075643A>C
Linked Data - Sequence & Population
gnomAD v2:
8:92075643 A / C
gnomAD v3:
8:91063415 A / C
gnomAD v4:
chr8-91063415-A-C
Joint Max Group AF
0.66776322 (AFR)
Genomes Max Group AF
0.66776322 (AFR)
Exomes Max Group AF
0.08884008 (NFE)
Linked Data - NCBI & NCI
dbSNP:
4493873
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.91063415A>C , CM000670.2:g.91063415A>C
GRCh38
NC_000008.10:g.92075643A>C , CM000670.1:g.92075643A>C
GRCh37
NC_000008.9:g.92144819A>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_110438.1:n.835T>G
Search 100 bp 5'
Search 100 bp 3'