ClinGen Allele Registry
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Canonical Allele Identifier:
CA184861805
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr8:g.118911634A>T
GRCh37
chr8:g.119923873A>T
Linked Data - Sequence & Population
gnomAD v2:
8:119923873 A / T
gnomAD v3:
8:118911634 A / T
gnomAD v4:
chr8-118911634-A-T
Joint Max Group AF
0.00303566 (EAS)
Genomes Max Group AF
0.00303566 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4355801
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.118911634A>T , CM000670.2:g.118911634A>T
GRCh38
NC_000008.10:g.119923873A>T , CM000670.1:g.119923873A>T
GRCh37
NC_000008.9:g.119993054A>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'