ClinGen Allele Registry
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Canonical Allele Identifier:
CA669684369
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.89067022A>T
GRCh37
chr10:g.90826779A>T
Linked Data - Sequence & Population
gnomAD v3:
10:89067022 A / T
gnomAD v4:
chr10-89067022-A-T
Linked Data - NCBI & NCI
dbSNP:
1937332
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.89067022A>T , CM000672.2:g.89067022A>T
GRCh38
NC_000010.10:g.90826779A>T , CM000672.1:g.90826779A>T
GRCh37
NC_000010.9:g.90816759A>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'