ClinGen Allele Registry
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Canonical Allele Identifier:
CA256493506
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr13:g.105545950T>A
GRCh37
chr13:g.106198299T>A
Linked Data - Sequence & Population
gnomAD v2:
13:106198299 T / A
gnomAD v3:
13:105545950 T / A
gnomAD v4:
chr13-105545950-T-A
Joint Max Group AF
0.0000325 (AFR)
Genomes Max Group AF
0.0000325 (AFR)
Linked Data - NCBI & NCI
dbSNP:
914799769
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.105545950T>A , CM000675.2:g.105545950T>A
GRCh38
NC_000013.10:g.106198299T>A , CM000675.1:g.106198299T>A
GRCh37
NC_000013.9:g.104996300T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'