ClinGen Allele Registry
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Canonical Allele Identifier:
CA216994975
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.1219991G>A
GRCh37
chr11:g.1241221G>A
Linked Data - Sequence & Population
gnomAD v2:
11:1241221 G / A
gnomAD v3:
11:1219991 G / A
gnomAD v4:
chr11-1219991-G-A
Joint Max Group AF
0.00078915 (AFR)
Genomes Max Group AF
0.00078915 (AFR)
Linked Data - NCBI & NCI
dbSNP:
35705950
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.1219991G>A , CM000673.2:g.1219991G>A
GRCh38
NC_000011.9:g.1241221G>A , CM000673.1:g.1241221G>A
GRCh37
NC_000011.8:g.1197797G>A
NCBI36
NG_031880.1:g.1927G>A
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