ClinGen Allele Registry
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Canonical Allele Identifier:
CA124882967
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr5:g.111079903G>T
GRCh37
chr5:g.110415601G>T
Linked Data - Sequence & Population
gnomAD v2:
5:110415601 G / T
gnomAD v3:
5:111079903 G / T
gnomAD v4:
chr5-111079903-G-T
Joint Max Group AF
0.07181214 (AFR)
Genomes Max Group AF
0.07181214 (AFR)
Linked Data - NCBI & NCI
dbSNP:
6886755
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.111079903G>T , CM000667.2:g.111079903G>T
GRCh38
NC_000005.9:g.110415601G>T , CM000667.1:g.110415601G>T
GRCh37
NC_000005.8:g.110443500G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'