ClinGen Allele Registry
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Canonical Allele Identifier:
CA600564199
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.81524052T>C
GRCh37
chr11:g.81235094T>C
Linked Data - Sequence & Population
gnomAD v2:
11:81235094 T / C
gnomAD v3:
11:81524052 T / C
gnomAD v4:
chr11-81524052-T-C
Joint Max Group AF
0.00001921 (AFR)
Genomes Max Group AF
0.00001921 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1242556857
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.81524052T>C , CM000673.2:g.81524052T>C
GRCh38
NC_000011.9:g.81235094T>C , CM000673.1:g.81235094T>C
GRCh37
NC_000011.8:g.80912742T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'