ClinGen Allele Registry
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Canonical Allele Identifier:
CA15941209
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.46346549G>T
GRCh37
chr19:g.46849806G>T
Linked Data - Sequence & Population
gnomAD v2:
19:46849806 G / T
gnomAD v3:
19:46346549 G / T
gnomAD v4:
chr19-46346549-G-T
Joint Max Group AF
0.29544611 (NFE)
Genomes Max Group AF
0.29544611 (NFE)
Linked Data - NCBI & NCI
dbSNP:
4802307
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.46346549G>T , CM000681.2:g.46346549G>T
GRCh38
NC_000019.9:g.46849806G>T , CM000681.1:g.46849806G>T
GRCh37
NC_000019.8:g.51541646G>T
NCBI36
NG_028163.1:g.4556G>T
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