ClinGen Allele Registry
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Canonical Allele Identifier:
CA10983781
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.51080468T>G
GRCh37
chr1:g.51546140T>G
Linked Data - Sequence & Population
gnomAD v2:
1:51546140 T / G
gnomAD v3:
1:51080468 T / G
gnomAD v4:
chr1-51080468-T-G
Joint Max Group AF
0.07113091 (AFR)
Genomes Max Group AF
0.07113091 (AFR)
Linked Data - NCBI & NCI
dbSNP:
17391905
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.51080468T>G , CM000663.2:g.51080468T>G
GRCh38
NC_000001.10:g.51546140T>G , CM000663.1:g.51546140T>G
GRCh37
NC_000001.9:g.51318728T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'