ClinGen Allele Registry
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Canonical Allele Identifier:
CA16441361
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.33548231T>C
GRCh37
chr12:g.33701166T>C
Linked Data - Sequence & Population
gnomAD v2:
12:33701166 T / C
gnomAD v3:
12:33548231 T / C
gnomAD v4:
chr12-33548231-T-C
Joint Max Group AF
0.80453842 (NFE)
Genomes Max Group AF
0.80453842 (NFE)
Linked Data - NCBI & NCI
dbSNP:
9300212
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.33548231T>C , CM000674.2:g.33548231T>C
GRCh38
NC_000012.11:g.33701166T>C , CM000674.1:g.33701166T>C
GRCh37
NC_000012.10:g.33592433T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'