ClinGen Allele Registry
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Canonical Allele Identifier:
CA885392423
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.109823461T>A
GRCh37
chr1:g.110366083T>A
Linked Data - Sequence & Population
gnomAD v3:
1:109823461 T / A
gnomAD v4:
chr1-109823461-T-A
Joint Max Group AF
0.000008 (AFR)
Genomes Max Group AF
0.000008 (AFR)
Linked Data - NCBI & NCI
dbSNP:
484959
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.109823461T>A , CM000663.2:g.109823461T>A
GRCh38
NC_000001.10:g.110366083T>A , CM000663.1:g.110366083T>A
GRCh37
NC_000001.9:g.110167606T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'