ClinGen Allele Registry
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Canonical Allele Identifier:
CA15755290
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.63136465C>T
GRCh37
chr12:g.63530245C>T
Linked Data - Sequence & Population
gnomAD v2:
12:63530245 C / T
gnomAD v3:
12:63136465 C / T
gnomAD v4:
chr12-63136465-C-T
Joint Max Group AF
0.12535864 (SAS)
Genomes Max Group AF
0.12535864 (SAS)
Linked Data - NCBI & NCI
dbSNP:
1587097
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.63136465C>T , CM000674.2:g.63136465C>T
GRCh38
NC_000012.11:g.63530245C>T , CM000674.1:g.63530245C>T
GRCh37
NC_000012.10:g.61816512C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'