ClinGen Allele Registry
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Canonical Allele Identifier:
CA14172948
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.78563924C>T
GRCh37
chr15:g.78856266C>T
Linked Data - Sequence & Population
gnomAD v2:
15:78856266 C / T
gnomAD v3:
15:78563924 C / T
gnomAD v4:
chr15-78563924-C-T
Joint Max Group AF
0.3639953 (NFE)
Genomes Max Group AF
0.3639953 (NFE)
Linked Data - NCBI & NCI
dbSNP:
3829787
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.78563924C>T , CM000677.2:g.78563924C>T
GRCh38
NC_000015.9:g.78856266C>T , CM000677.1:g.78856266C>T
GRCh37
NC_000015.8:g.76643321C>T
NCBI36
NG_023328.1:g.3405C>T
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