ClinGen Allele Registry
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Canonical Allele Identifier:
CA14505322
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr17:g.77008131A>T
GRCh37
chr17:g.75004213A>T
Linked Data - Sequence & Population
gnomAD v2:
17:75004213 A / T
gnomAD v3:
17:77008131 A / T
gnomAD v4:
chr17-77008131-A-T
Joint Max Group AF
0.13368341 (AMR)
Genomes Max Group AF
0.13368341 (AMR)
Linked Data - NCBI & NCI
dbSNP:
11653989
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.77008131A>T , CM000679.2:g.77008131A>T
GRCh38
NC_000017.10:g.75004213A>T , CM000679.1:g.75004213A>T
GRCh37
NC_000017.9:g.72515808A>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'