ClinGen Allele Registry
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Canonical Allele Identifier:
CA30986604
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.156060246C>T
GRCh37
chr1:g.156030037C>T
Linked Data - Sequence & Population
gnomAD v2:
1:156030037 C / T
gnomAD v3:
1:156060246 C / T
gnomAD v4:
chr1-156060246-C-T
Joint Max Group AF
0.01871735 (NFE)
Genomes Max Group AF
0.01871735 (NFE)
Linked Data - NCBI & NCI
dbSNP:
34372695
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.156060246C>T , CM000663.2:g.156060246C>T
GRCh38
NC_000001.10:g.156030037C>T , CM000663.1:g.156030037C>T
GRCh37
NC_000001.9:g.154296661C>T
NCBI36
NG_009898.1:g.10521C>T , LRG_81:g.10521C>T
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