ClinGen Allele Registry
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Canonical Allele Identifier:
CA12927288
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.31638152A>T
GRCh37
chr8:g.31495668A>T
Linked Data - Sequence & Population
gnomAD v2:
8:31495668 A / T
gnomAD v3:
8:31638152 A / T
gnomAD v4:
chr8-31638152-A-T
Joint Max Group AF
0.74726347 (NFE)
Genomes Max Group AF
0.74726347 (NFE)
Linked Data - NCBI & NCI
dbSNP:
7014762
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.31638152A>T , CM000670.2:g.31638152A>T
GRCh38
NC_000008.10:g.31495668A>T , CM000670.1:g.31495668A>T
GRCh37
NC_000008.9:g.31615210A>T
NCBI36
NG_012005.1:g.3401A>T
NG_012005.2:g.3931A>T
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