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Canonical Allele Identifier:
CA13471024
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.114019631T>C
GRCh37
chr11:g.113890353T>C
Linked Data - Sequence & Population
gnomAD v2:
11:113890353 T / C
gnomAD v3:
11:114019631 T / C
gnomAD v4:
chr11-114019631-T-C
Joint Max Group AF
0.18594024 (EAS)
Genomes Max Group AF
0.18594024 (EAS)
Linked Data - NCBI & NCI
dbSNP:
12221649
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.114019631T>C , CM000673.2:g.114019631T>C
GRCh38
NC_000011.9:g.113890353T>C , CM000673.1:g.113890353T>C
GRCh37
NC_000011.8:g.113395563T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'