ClinGen Allele Registry
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Canonical Allele Identifier:
CA14765801
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr20:g.63343128G>A
GRCh37
chr20:g.61974480G>A
Linked Data - Sequence & Population
gnomAD v2:
20:61974480 G / A
gnomAD v3:
20:63343128 G / A
gnomAD v4:
chr20-63343128-G-A
Joint Max Group AF
0.63666906 (NFE)
Genomes Max Group AF
0.63166082 (NFE)
Exomes Max Group AF
0.63775483 (NFE)
Linked Data - NCBI & NCI
dbSNP:
4522666
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.63343128G>A , CM000682.2:g.63343128G>A
GRCh38
NC_000020.10:g.61974480G>A , CM000682.1:g.61974480G>A
GRCh37
NC_000020.9:g.61444924G>A
NCBI36
NG_011931.1:g.23216C>T
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