ClinGen Allele Registry
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Canonical Allele Identifier:
CA10716938
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.17307077G>T
GRCh37
chr1:g.17633572G>T
Linked Data - Sequence & Population
gnomAD v2:
1:17633572 G / T
gnomAD v3:
1:17307077 G / T
gnomAD v4:
chr1-17307077-G-T
Joint Max Group AF
0.84256563 (EAS)
Genomes Max Group AF
0.84256563 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2477134
2100240509
2100240522
2100240544
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.17307077G>T , CM000663.2:g.17307077G>T
GRCh38
NC_000001.10:g.17633572G>T , CM000663.1:g.17633572G>T
GRCh37
NC_000001.9:g.17506159G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'