ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA13355577
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.94922089G>A
GRCh37
chr10:g.96681846G>A
Linked Data - Sequence & Population
gnomAD v2:
10:96681846 G / A
gnomAD v3:
10:94922089 G / A
gnomAD v4:
chr10-94922089-G-A
Joint Max Group AF
0.30421904 (SAS)
Genomes Max Group AF
0.30421904 (SAS)
Linked Data - NCBI & NCI
dbSNP:
1074145
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.94922089G>A , CM000672.2:g.94922089G>A
GRCh38
NC_000010.10:g.96681846G>A , CM000672.1:g.96681846G>A
GRCh37
NC_000010.9:g.96671836G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'