ClinGen Allele Registry
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Canonical Allele Identifier:
CA14193103
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.34713685T>A
GRCh37
chr15:g.35005886T>A
Linked Data - Sequence & Population
gnomAD v2:
15:35005886 T / A
gnomAD v3:
15:34713685 T / A
gnomAD v4:
chr15-34713685-T-A
Joint Max Group AF
0.5968862 (SAS)
Genomes Max Group AF
0.5968862 (SAS)
Linked Data - NCBI & NCI
dbSNP:
524952
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.34713685T>A , CM000677.2:g.34713685T>A
GRCh38
NC_000015.9:g.35005886T>A , CM000677.1:g.35005886T>A
GRCh37
NC_000015.8:g.32793178T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'