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Canonical Allele Identifier:
CA50646131
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.76013235G>T
GRCh37
chr2:g.76240361G>T
Linked Data - Sequence & Population
gnomAD v2:
2:76240361 G / T
gnomAD v3:
2:76013235 G / T
gnomAD v4:
chr2-76013235-G-T
Joint Max Group AF
0.43088952 (SAS)
Genomes Max Group AF
0.43088952 (SAS)
Linked Data - NCBI & NCI
dbSNP:
436000
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.76013235G>T , CM000664.2:g.76013235G>T
GRCh38
NC_000002.11:g.76240361G>T , CM000664.1:g.76240361G>T
GRCh37
NC_000002.10:g.76093869G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'