ClinGen Allele Registry
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Canonical Allele Identifier:
CA36468615
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr1:g.205783537A>G
GRCh37
chr1:g.205752665A>G
Linked Data - Sequence & Population
gnomAD v2:
1:205752665 A / G
gnomAD v3:
1:205783537 A / G
gnomAD v4:
chr1-205783537-A-G
Joint Max Group AF
0.75392969 (NFE)
Genomes Max Group AF
0.75392969 (NFE)
Linked Data - NCBI & NCI
dbSNP:
947211
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.205783537A>G , CM000663.2:g.205783537A>G
GRCh38
NC_000001.10:g.205752665A>G , CM000663.1:g.205752665A>G
GRCh37
NC_000001.9:g.204019288A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_922472.1:n.889A>G
Search 100 bp 5'
Search 100 bp 3'