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Canonical Allele Identifier:
CA13400939
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.123742322C>T
GRCh37
chr11:g.123613030C>T
Linked Data - Sequence & Population
gnomAD v2:
11:123613030 C / T
gnomAD v3:
11:123742322 C / T
gnomAD v4:
chr11-123742322-C-T
Joint Max Group AF
0.73162936 (MID)
Genomes Max Group AF
0.69032762 (NFE)
Linked Data - NCBI & NCI
dbSNP:
10893081
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.123742322C>T , CM000673.2:g.123742322C>T
GRCh38
NC_000011.9:g.123613030C>T , CM000673.1:g.123613030C>T
GRCh37
NC_000011.8:g.123118240C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'