ClinGen Allele Registry
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Canonical Allele Identifier:
CA12473933
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.81774578G>T
GRCh37
chr7:g.81403894G>T
Linked Data - Sequence & Population
gnomAD v2:
7:81403894 G / T
gnomAD v3:
7:81774578 G / T
gnomAD v4:
chr7-81774578-G-T
Joint Max Group AF
0.11063683 (NFE)
Genomes Max Group AF
0.11063683 (NFE)
Linked Data - NCBI & NCI
dbSNP:
17501108
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.81774578G>T , CM000669.2:g.81774578G>T
GRCh38
NC_000007.13:g.81403894G>T , CM000669.1:g.81403894G>T
GRCh37
NC_000007.12:g.81241830G>T
NCBI36
NG_016274.1:g.559C>A
NG_016274.2:g.559C>A
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