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Canonical Allele Identifier:
CA116349031
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.28340139T>A
GRCh37
chr5:g.28340246T>A
Linked Data - Sequence & Population
gnomAD v3:
5:28340139 T / A
gnomAD v4:
chr5-28340139-T-A
Joint Max Group AF
0.00000801 (AFR)
Genomes Max Group AF
0.00000801 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1014874156
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.28340139T>A , CM000667.2:g.28340139T>A
GRCh38
NC_000005.9:g.28340246T>A , CM000667.1:g.28340246T>A
GRCh37
NC_000005.8:g.28376003T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'