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Canonical Allele Identifier:
CA15890170
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr16:g.85977731C>T
GRCh37
chr16:g.86011337C>T
Linked Data - Sequence & Population
gnomAD v2:
16:86011337 C / T
gnomAD v3:
16:85977731 C / T
gnomAD v4:
chr16-85977731-C-T
Joint Max Group AF
0.09312397 (NFE)
Genomes Max Group AF
0.09312397 (NFE)
Linked Data - NCBI & NCI
dbSNP:
10521318
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.85977731C>T , CM000678.2:g.85977731C>T
GRCh38
NC_000016.9:g.86011337C>T , CM000678.1:g.86011337C>T
GRCh37
NC_000016.8:g.84568838C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'