ClinGen Allele Registry
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Canonical Allele Identifier:
CA13793708
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr13:g.78664790G>A
GRCh37
chr13:g.79238925G>A
Linked Data - Sequence & Population
gnomAD v2:
13:79238925 G / A
gnomAD v3:
13:78664790 G / A
gnomAD v4:
chr13-78664790-G-A
Joint Max Group AF
0.61371351 (MID)
Genomes Max Group AF
0.57115449 (NFE)
Linked Data - NCBI & NCI
dbSNP:
4304924
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.78664790G>A , CM000675.2:g.78664790G>A
GRCh38
NC_000013.10:g.79238925G>A , CM000675.1:g.79238925G>A
GRCh37
NC_000013.9:g.78136926G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'