ClinGen Allele Registry
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Canonical Allele Identifier:
CA251307960
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr13:g.69449553C>T
GRCh37
chr13:g.70023685C>T
Linked Data - Sequence & Population
gnomAD v2:
13:70023685 C / T
gnomAD v3:
13:69449553 C / T
gnomAD v4:
chr13-69449553-C-T
Joint Max Group AF
0.9934621 (NFE)
Genomes Max Group AF
0.9934621 (NFE)
Linked Data - NCBI & NCI
dbSNP:
352236
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.69449553C>T , CM000675.2:g.69449553C>T
GRCh38
NC_000013.10:g.70023685C>T , CM000675.1:g.70023685C>T
GRCh37
NC_000013.9:g.68921686C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'