ClinGen Allele Registry
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Canonical Allele Identifier:
CA11061096
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.26559753C>T
GRCh37
chr2:g.26782621C>T
Linked Data - Sequence & Population
gnomAD v2:
2:26782621 C / T
gnomAD v3:
2:26559753 C / T
gnomAD v4:
chr2-26559753-C-T
Joint Max Group AF
0.42889105 (AMR)
Genomes Max Group AF
0.42889105 (AMR)
Linked Data - NCBI & NCI
dbSNP:
1011108
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.26559753C>T , CM000664.2:g.26559753C>T
GRCh38
NC_000002.11:g.26782621C>T , CM000664.1:g.26782621C>T
GRCh37
NC_000002.10:g.26636125C>T
NCBI36
NG_009937.1:g.3946G>A
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