ClinGen Allele Registry
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Canonical Allele Identifier:
CA116087940
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.26139029A>T
GRCh37
chr5:g.26139138A>T
Linked Data - Sequence & Population
gnomAD v2:
5:26139138 A / T
gnomAD v3:
5:26139029 A / T
gnomAD v4:
chr5-26139029-A-T
Joint Max Group AF
0.12404647 (AFR)
Genomes Max Group AF
0.12404647 (AFR)
Linked Data - NCBI & NCI
dbSNP:
4701523
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.26139029A>T , CM000667.2:g.26139029A>T
GRCh38
NC_000005.9:g.26139138A>T , CM000667.1:g.26139138A>T
GRCh37
NC_000005.8:g.26174895A>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'