ClinGen Allele Registry
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Canonical Allele Identifier:
CA14368136
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.1761607G>A
GRCh37
chr17:g.1664901G>A
Linked Data - Sequence & Population
gnomAD v2:
17:1664901 G / A
gnomAD v3:
17:1761607 G / A
gnomAD v4:
chr17-1761607-G-A
Joint Max Group AF
0.36713663 (NFE)
Genomes Max Group AF
0.36713663 (NFE)
Linked Data - NCBI & NCI
dbSNP:
12948385
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.1761607G>A , CM000679.2:g.1761607G>A
GRCh38
NC_000017.10:g.1664901G>A , CM000679.1:g.1664901G>A
GRCh37
NC_000017.9:g.1611651G>A
NCBI36
NG_028180.1:g.4643G>A
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