ClinGen Allele Registry
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Canonical Allele Identifier:
CA123949742
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.100613278A>T
GRCh37
chr5:g.99948982A>T
Linked Data - Sequence & Population
gnomAD v2:
5:99948982 A / T
gnomAD v3:
5:100613278 A / T
gnomAD v4:
chr5-100613278-A-T
Joint Max Group AF
0.84855492 (AMR)
Genomes Max Group AF
0.84855492 (AMR)
Linked Data - NCBI & NCI
dbSNP:
383830
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.100613278A>T , CM000667.2:g.100613278A>T
GRCh38
NC_000005.9:g.99948982A>T , CM000667.1:g.99948982A>T
GRCh37
NC_000005.8:g.99976881A>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'