ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA233335383
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.17567834G>T
GRCh37
chr12:g.17720768G>T
Linked Data - Sequence & Population
gnomAD v2:
12:17720768 G / T
gnomAD v3:
12:17567834 G / T
gnomAD v4:
chr12-17567834-G-T
Joint Max Group AF
0.26305378 (MID)
Genomes Max Group AF
0.25509173 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1163763
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.17567834G>T , CM000674.2:g.17567834G>T
GRCh38
NC_000012.11:g.17720768G>T , CM000674.1:g.17720768G>T
GRCh37
NC_000012.10:g.17612035G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'