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Canonical Allele Identifier:
CA15704249
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.34583888T>G
GRCh37
chr11:g.34605435T>G
Linked Data - Sequence & Population
gnomAD v2:
11:34605435 T / G
gnomAD v3:
11:34583888 T / G
gnomAD v4:
chr11-34583888-T-G
Joint Max Group AF
0.79595456 (NFE)
Genomes Max Group AF
0.79595456 (NFE)
Linked Data - NCBI & NCI
dbSNP:
5028798
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.34583888T>G , CM000673.2:g.34583888T>G
GRCh38
NC_000011.9:g.34605435T>G , CM000673.1:g.34605435T>G
GRCh37
NC_000011.8:g.34562011T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'