ClinGen Allele Registry
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Canonical Allele Identifier:
CA16410439
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.13552278A>C
GRCh37
chr11:g.13573825A>C
Linked Data - Sequence & Population
gnomAD v2:
11:13573825 A / C
gnomAD v3:
11:13552278 A / C
gnomAD v4:
chr11-13552278-A-C
Joint Max Group AF
0.34575094 (NFE)
Genomes Max Group AF
0.34575094 (NFE)
Linked Data - NCBI & NCI
dbSNP:
10500784
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.13552278A>C , CM000673.2:g.13552278A>C
GRCh38
NC_000011.9:g.13573825A>C , CM000673.1:g.13573825A>C
GRCh37
NC_000011.8:g.13530401A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'