ClinGen Allele Registry
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Canonical Allele Identifier:
CA11928226
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr5:g.50937365T>C
GRCh37
chr5:g.50233199T>C
Linked Data - Sequence & Population
gnomAD v2:
5:50233199 T / C
gnomAD v3:
5:50937365 T / C
gnomAD v4:
chr5-50937365-T-C
Joint Max Group AF
0.8341535 (EAS)
Genomes Max Group AF
0.8341535 (EAS)
Linked Data - NCBI & NCI
dbSNP:
151997
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.50937365T>C , CM000667.2:g.50937365T>C
GRCh38
NC_000005.9:g.50233199T>C , CM000667.1:g.50233199T>C
GRCh37
NC_000005.8:g.50268956T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'