ClinGen Allele Registry
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Canonical Allele Identifier:
CA14767318
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr20:g.2774842T>C
GRCh37
chr20:g.2755488T>C
Linked Data - Sequence & Population
gnomAD v2:
20:2755488 T / C
gnomAD v3:
20:2774842 T / C
gnomAD v4:
chr20-2774842-T-C
Joint Max Group AF
0.17230187 (NFE)
Genomes Max Group AF
0.17230187 (NFE)
Linked Data - NCBI & NCI
dbSNP:
6138892
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.2774842T>C , CM000682.2:g.2774842T>C
GRCh38
NC_000020.10:g.2755488T>C , CM000682.1:g.2755488T>C
GRCh37
NC_000020.9:g.2703488T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'