ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA14412386
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.78315910T>G
GRCh37
chr17:g.76311991T>G
Linked Data - Sequence & Population
gnomAD v2:
17:76311991 T / G
gnomAD v3:
17:78315910 T / G
gnomAD v4:
chr17-78315910-T-G
Joint Max Group AF
0.65316849 (EAS)
Genomes Max Group AF
0.65335075 (EAS)
Exomes Max Group AF
0.273776 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4789580
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.78315910T>G , CM000679.2:g.78315910T>G
GRCh38
NC_000017.10:g.76311991T>G , CM000679.1:g.76311991T>G
GRCh37
NC_000017.9:g.73823586T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'