ClinGen Allele Registry
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Canonical Allele Identifier:
CA13273599
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.99514608G>A
GRCh37
chr10:g.101274365G>A
Linked Data - Sequence & Population
gnomAD v2:
10:101274365 G / A
gnomAD v3:
10:99514608 G / A
gnomAD v4:
chr10-99514608-G-A
Joint Max Group AF
0.51553111 (EAS)
Genomes Max Group AF
0.51553111 (EAS)
Linked Data - NCBI & NCI
dbSNP:
7078219
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.99514608G>A , CM000672.2:g.99514608G>A
GRCh38
NC_000010.10:g.101274365G>A , CM000672.1:g.101274365G>A
GRCh37
NC_000010.9:g.101264355G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'