ClinGen Allele Registry
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Canonical Allele Identifier:
CA10782215
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr1:g.159715306C>T
GRCh37
chr1:g.159685096C>T
Linked Data - Sequence & Population
gnomAD v2:
1:159685096 C / T
gnomAD v3:
1:159715306 C / T
gnomAD v4:
chr1-159715306-C-T
Joint Max Group AF
0.84705898 (AFR)
Genomes Max Group AF
0.84705898 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2794521
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.159715306C>T , CM000663.2:g.159715306C>T
GRCh38
NC_000001.10:g.159685096C>T , CM000663.1:g.159685096C>T
GRCh37
NC_000001.9:g.157951720C>T
NCBI36
NG_013007.1:g.4284G>A
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