ClinGen Allele Registry
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Canonical Allele Identifier:
CA14075649
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.32712046G>A
GRCh37
chr15:g.33004247G>A
Linked Data - Sequence & Population
gnomAD v2:
15:33004247 G / A
gnomAD v3:
15:32712046 G / A
gnomAD v4:
chr15-32712046-G-A
Joint Max Group AF
0.76067317 (EAS)
Genomes Max Group AF
0.76067317 (EAS)
Linked Data - NCBI & NCI
dbSNP:
11632715
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.32712046G>A , CM000677.2:g.32712046G>A
GRCh38
NC_000015.9:g.33004247G>A , CM000677.1:g.33004247G>A
GRCh37
NC_000015.8:g.30791539G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'