ClinGen Allele Registry
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Canonical Allele Identifier:
CA11936683
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.91466931G>A
GRCh37
chr5:g.90762748G>A
Linked Data - Sequence & Population
gnomAD v2:
5:90762748 G / A
gnomAD v3:
5:91466931 G / A
gnomAD v4:
chr5-91466931-G-A
Joint Max Group AF
0.68947111 (AFR)
Genomes Max Group AF
0.68947111 (AFR)
Linked Data - NCBI & NCI
dbSNP:
933688
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.91466931G>A , CM000667.2:g.91466931G>A
GRCh38
NC_000005.9:g.90762748G>A , CM000667.1:g.90762748G>A
GRCh37
NC_000005.8:g.90798504G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'