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Canonical Allele Identifier:
CA31391112
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.159714894C>T
GRCh37
chr1:g.159684684C>T
Linked Data - Sequence & Population
gnomAD v2:
1:159684684 C / T
gnomAD v3:
1:159714894 C / T
gnomAD v4:
chr1-159714894-C-T
Joint Max Group AF
0.16548296 (AFR)
Genomes Max Group AF
0.16548296 (AFR)
Linked Data - NCBI & NCI
dbSNP:
3093062
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.159714894C>T , CM000663.2:g.159714894C>T
GRCh38
NC_000001.10:g.159684684C>T , CM000663.1:g.159684684C>T
GRCh37
NC_000001.9:g.157951308C>T
NCBI36
NG_013007.1:g.4696G>A
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