ClinGen Allele Registry
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Canonical Allele Identifier:
CA16047344
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.17307027G>A
GRCh37
chr1:g.17633522G>A
Linked Data - Sequence & Population
gnomAD v2:
1:17633522 G / A
gnomAD v3:
1:17307027 G / A
gnomAD v4:
chr1-17307027-G-A
Joint Max Group AF
0.99244208 (NFE)
Genomes Max Group AF
0.99244208 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2501796
2100212506
2100212514
2100212525
2100212544
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.17307027G>A , CM000663.2:g.17307027G>A
GRCh38
NC_000001.10:g.17633522G>A , CM000663.1:g.17633522G>A
GRCh37
NC_000001.9:g.17506109G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'