ClinGen Allele Registry
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Canonical Allele Identifier:
CA14142165
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.32758222C>T
GRCh37
chr15:g.33050423C>T
Linked Data - Sequence & Population
gnomAD v2:
15:33050423 C / T
gnomAD v3:
15:32758222 C / T
gnomAD v4:
chr15-32758222-C-T
Joint Max Group AF
0.67134477 (NFE)
Genomes Max Group AF
0.67134477 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1258763
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.32758222C>T , CM000677.2:g.32758222C>T
GRCh38
NC_000015.9:g.33050423C>T , CM000677.1:g.33050423C>T
GRCh37
NC_000015.8:g.30837715C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'