ClinGen Allele Registry
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Canonical Allele Identifier:
CA15855779
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr15:g.60317231C>T
GRCh37
chr15:g.60609430C>T
Linked Data - Sequence & Population
gnomAD v2:
15:60609430 C / T
gnomAD v3:
15:60317231 C / T
gnomAD v4:
chr15-60317231-C-T
Joint Max Group AF
0.55396511 (AMR)
Genomes Max Group AF
0.55396511 (AMR)
Linked Data - NCBI & NCI
dbSNP:
11853426
2140573449
2140573455
2140573461
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.60317231C>T , CM000677.2:g.60317231C>T
GRCh38
NC_000015.9:g.60609430C>T , CM000677.1:g.60609430C>T
GRCh37
NC_000015.8:g.58396722C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'