ClinGen Allele Registry
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Canonical Allele Identifier:
CA256493494
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr13:g.105545936A>G
GRCh37
chr13:g.106198285A>G
Linked Data - Sequence & Population
gnomAD v2:
13:106198285 A / G
gnomAD v3:
13:105545936 A / G
gnomAD v4:
chr13-105545936-A-G
Joint Max Group AF
0.00001171 (NFE)
Genomes Max Group AF
0.00001171 (NFE)
Linked Data - NCBI & NCI
dbSNP:
993680785
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.105545936A>G , CM000675.2:g.105545936A>G
GRCh38
NC_000013.10:g.106198285A>G , CM000675.1:g.106198285A>G
GRCh37
NC_000013.9:g.104996286A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'