ClinGen Allele Registry
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Canonical Allele Identifier:
CA239689117
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.73435176C>T
GRCh37
chr12:g.73828956C>T
Linked Data - Sequence & Population
gnomAD v2:
12:73828956 C / T
gnomAD v3:
12:73435176 C / T
gnomAD v4:
chr12-73435176-C-T
Joint Max Group AF
0.7489441 (EAS)
Genomes Max Group AF
0.7489441 (EAS)
Linked Data - NCBI & NCI
dbSNP:
7963521
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.73435176C>T , CM000674.2:g.73435176C>T
GRCh38
NC_000012.11:g.73828956C>T , CM000674.1:g.73828956C>T
GRCh37
NC_000012.10:g.72115223C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'