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Canonical Allele Identifier:
CA690788098
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.63154856C>T
GRCh37
chr12:g.63548636C>T
Linked Data - Sequence & Population
gnomAD v3:
12:63154856 C / T
gnomAD v4:
chr12-63154856-C-T
Joint Max Group AF
0.0002819 (SAS)
Genomes Max Group AF
0.0002819 (SAS)
Linked Data - NCBI & NCI
dbSNP:
1363843362
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.63154856C>T , CM000674.2:g.63154856C>T
GRCh38
NC_000012.11:g.63548636C>T , CM000674.1:g.63548636C>T
GRCh37
NC_000012.10:g.61834903C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'