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Canonical Allele Identifier:
CA16456432
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.114908619C>T
GRCh37
chr12:g.115346424C>T
Linked Data - Sequence & Population
gnomAD v2:
12:115346424 C / T
gnomAD v3:
12:114908619 C / T
gnomAD v4:
chr12-114908619-C-T
Joint Max Group AF
0.7511369 (AFR)
Genomes Max Group AF
0.7511369 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1896312
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.114908619C>T , CM000674.2:g.114908619C>T
GRCh38
NC_000012.11:g.115346424C>T , CM000674.1:g.115346424C>T
GRCh37
NC_000012.10:g.113830807C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'