ClinGen Allele Registry
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Canonical Allele Identifier:
CA248323972
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr13:g.34080781A>G
GRCh37
chr13:g.34654918A>G
Linked Data - Sequence & Population
gnomAD v2:
13:34654918 A / G
gnomAD v3:
13:34080781 A / G
gnomAD v4:
13:34080781 A / G
Linked Data - NCBI & NCI
dbSNP:
690705
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.34080781A>G , CM000675.2:g.34080781A>G
GRCh38
NC_000013.10:g.34654918A>G , CM000675.1:g.34654918A>G
GRCh37
NC_000013.9:g.33552918A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'