ClinGen Allele Registry
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Canonical Allele Identifier:
CA15538658
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.89792100C>T
GRCh37
chr8:g.90804328C>T
Linked Data - Sequence & Population
gnomAD v2:
8:90804328 C / T
gnomAD v3:
8:89792100 C / T
gnomAD v4:
chr8-89792100-C-T
Joint Max Group AF
0.68162273 (AFR)
Genomes Max Group AF
0.68162273 (AFR)
Linked Data - NCBI & NCI
dbSNP:
383592
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.89792100C>T , CM000670.2:g.89792100C>T
GRCh38
NC_000008.10:g.90804328C>T , CM000670.1:g.90804328C>T
GRCh37
NC_000008.9:g.90873469C>T
NCBI36
NG_033016.1:g.39354C>T
NG_033016.2:g.39354C>T
Search 100 bp 5'
Search 100 bp 3'