ClinGen Allele Registry
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Canonical Allele Identifier:
CA12110596
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.1445501A>T
GRCh37
chr5:g.1445616A>T
Linked Data - Sequence & Population
gnomAD v2:
5:1445616 A / T
gnomAD v3:
5:1445501 A / T
gnomAD v4:
chr5-1445501-A-T
Joint Max Group AF
0.59250748 (NFE)
Genomes Max Group AF
0.59070298 (NFE)
Exomes Max Group AF
0.59277718 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2975226
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.1445501A>T , CM000667.2:g.1445501A>T
GRCh38
NC_000005.9:g.1445616A>T , CM000667.1:g.1445616A>T
GRCh37
NC_000005.8:g.1498616A>T
NCBI36
NG_015885.1:g.4928T>A
Search 100 bp 5'
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