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Canonical Allele Identifier:
CA13119742
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr9:g.112925455T>C
GRCh37
chr9:g.115687735T>C
Linked Data - Sequence & Population
gnomAD v2:
9:115687735 T / C
gnomAD v3:
9:112925455 T / C
gnomAD v4:
chr9-112925455-T-C
Joint Max Group AF
0.13071404 (NFE)
Genomes Max Group AF
0.13071404 (NFE)
Linked Data - NCBI & NCI
dbSNP:
10817408
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.112925455T>C , CM000671.2:g.112925455T>C
GRCh38
NC_000009.11:g.115687735T>C , CM000671.1:g.115687735T>C
GRCh37
NC_000009.10:g.114727556T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'