ClinGen Allele Registry
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Canonical Allele Identifier:
CA121860635
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.81791715G>T
GRCh37
chr5:g.81087534G>T
Linked Data - Sequence & Population
gnomAD v2:
5:81087534 G / T
gnomAD v3:
5:81791715 G / T
gnomAD v4:
chr5-81791715-G-T
Joint Max Group AF
0.79878889 (AFR)
Genomes Max Group AF
0.79878889 (AFR)
Linked Data - NCBI & NCI
dbSNP:
410644
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.81791715G>T , CM000667.2:g.81791715G>T
GRCh38
NC_000005.9:g.81087534G>T , CM000667.1:g.81087534G>T
GRCh37
NC_000005.8:g.81123290G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'