ClinGen Allele Registry
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Canonical Allele Identifier:
CA14110609
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr15:g.90868426C>T
GRCh37
chr15:g.91411656C>T
Linked Data - Sequence & Population
gnomAD v2:
15:91411656 C / T
gnomAD v3:
15:90868426 C / T
gnomAD v4:
chr15-90868426-C-T
Joint Max Group AF
0.35232021 (NFE)
Genomes Max Group AF
0.35232021 (NFE)
Linked Data - NCBI & NCI
dbSNP:
4932178
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.90868426C>T , CM000677.2:g.90868426C>T
GRCh38
NC_000015.9:g.91411656C>T , CM000677.1:g.91411656C>T
GRCh37
NC_000015.8:g.89212660C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'