ClinGen Allele Registry
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Canonical Allele Identifier:
CA12165730
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.1447726G>A
GRCh37
chr5:g.1447841G>A
Linked Data - Sequence & Population
gnomAD v2:
5:1447841 G / A
gnomAD v3:
5:1447726 G / A
gnomAD v4:
chr5-1447726-G-A
Joint Max Group AF
0.26944732 (SAS)
Genomes Max Group AF
0.26944732 (SAS)
Linked Data - NCBI & NCI
dbSNP:
2550956
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.1447726G>A , CM000667.2:g.1447726G>A
GRCh38
NC_000005.9:g.1447841G>A , CM000667.1:g.1447841G>A
GRCh37
NC_000005.8:g.1500841G>A
NCBI36
NG_015885.1:g.2703C>T
Search 100 bp 5'
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