ClinGen Allele Registry
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Canonical Allele Identifier:
CA15790465
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr13:g.34032049A>G
GRCh37
chr13:g.34606186A>G
Linked Data - Sequence & Population
gnomAD v2:
13:34606186 A / G
gnomAD v3:
13:34032049 A / G
gnomAD v4:
chr13-34032049-A-G
Joint Max Group AF
0.20998377 (AFR)
Genomes Max Group AF
0.20998377 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2321744
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.34032049A>G , CM000675.2:g.34032049A>G
GRCh38
NC_000013.10:g.34606186A>G , CM000675.1:g.34606186A>G
GRCh37
NC_000013.9:g.33504186A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_001749817.1:n.1515T>C
Search 100 bp 5'
Search 100 bp 3'