ClinGen Allele Registry
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Canonical Allele Identifier:
CA801838528
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.110854359T>A
GRCh37
chr5:g.110190058T>A
Linked Data - Sequence & Population
gnomAD v3:
5:110854359 T / A
gnomAD v4:
chr5-110854359-T-A
Joint Max Group AF
0.000008 (AFR)
Genomes Max Group AF
0.000008 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1305688976
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.110854359T>A , CM000667.2:g.110854359T>A
GRCh38
NC_000005.9:g.110190058T>A , CM000667.1:g.110190058T>A
GRCh37
NC_000005.8:g.110217957T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'