ClinGen Allele Registry
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Canonical Allele Identifier:
CA14788441
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr20:g.43193056G>A
GRCh37
chr20:g.41821696G>A
Linked Data - Sequence & Population
gnomAD v2:
20:41821696 G / A
gnomAD v3:
20:43193056 G / A
gnomAD v4:
chr20-43193056-G-A
Joint Max Group AF
0.2441421 (NFE)
Genomes Max Group AF
0.2441421 (NFE)
Linked Data - NCBI & NCI
dbSNP:
13036957
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.43193056G>A , CM000682.2:g.43193056G>A
GRCh38
NC_000020.10:g.41821696G>A , CM000682.1:g.41821696G>A
GRCh37
NC_000020.9:g.41255110G>A
NCBI36
NG_033880.1:g.1862C>T
NG_033880.2:g.1862C>T
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