ClinGen Allele Registry
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Canonical Allele Identifier:
CA12321542
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.32607747G>T
GRCh37
chr6:g.32575524G>T
Linked Data - Sequence & Population
gnomAD v2:
6:32575524 G / T
gnomAD v3:
6:32607747 G / T
gnomAD v4:
chr6-32607747-G-T
Joint Max Group AF
0.29559593 (SAS)
Genomes Max Group AF
0.29559593 (SAS)
Linked Data - NCBI & NCI
dbSNP:
4713555
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.32607747G>T , CM000668.2:g.32607747G>T
GRCh38
NC_000006.11:g.32575524G>T , CM000668.1:g.32575524G>T
GRCh37
NC_000006.10:g.32683502G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'