ClinGen Allele Registry
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Canonical Allele Identifier:
CA10787174
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.199936700C>T
GRCh37
chr1:g.199905828C>T
Linked Data - Sequence & Population
gnomAD v2:
1:199905828 C / T
gnomAD v3:
1:199936700 C / T
gnomAD v4:
chr1-199936700-C-T
Joint Max Group AF
0.74538822 (EAS)
Genomes Max Group AF
0.74538822 (EAS)
Linked Data - NCBI & NCI
dbSNP:
12029406
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.199936700C>T , CM000663.2:g.199936700C>T
GRCh38
NC_000001.10:g.199905828C>T , CM000663.1:g.199905828C>T
GRCh37
NC_000001.9:g.198172451C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'