ClinGen Allele Registry
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Canonical Allele Identifier:
CA14303531
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.81230992T>G
GRCh37
chr16:g.81264597T>G
Linked Data - Sequence & Population
gnomAD v2:
16:81264597 T / G
gnomAD v3:
16:81230992 T / G
gnomAD v4:
chr16-81230992-T-G
Joint Max Group AF
0.79465167 (EAS)
Genomes Max Group AF
0.79465167 (EAS)
Linked Data - NCBI & NCI
dbSNP:
6564851
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.81230992T>G , CM000678.2:g.81230992T>G
GRCh38
NC_000016.9:g.81264597T>G , CM000678.1:g.81264597T>G
GRCh37
NC_000016.8:g.79822098T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'