ClinGen Allele Registry
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Canonical Allele Identifier:
CA14849642
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr20:g.57636797T>C
GRCh37
chr20:g.56211853T>C
Linked Data - Sequence & Population
gnomAD v2:
20:56211853 T / C
gnomAD v3:
20:57636797 T / C
gnomAD v4:
chr20-57636797-T-C
Joint Max Group AF
0.82874141 (NFE)
Genomes Max Group AF
0.82874141 (NFE)
Linked Data - NCBI & NCI
dbSNP:
6128112
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.57636797T>C , CM000682.2:g.57636797T>C
GRCh38
NC_000020.10:g.56211853T>C , CM000682.1:g.56211853T>C
GRCh37
NC_000020.9:g.55645259T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'