ClinGen Allele Registry
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Canonical Allele Identifier:
CA700746701
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr13:g.73342491C>G
GRCh37
chr13:g.73916628C>G
Linked Data - Sequence & Population
gnomAD v3:
13:73342491 C / G
gnomAD v4:
chr13-73342491-C-G
Linked Data - NCBI & NCI
dbSNP:
9543325
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.73342491C>G , CM000675.2:g.73342491C>G
GRCh38
NC_000013.10:g.73916628C>G , CM000675.1:g.73916628C>G
GRCh37
NC_000013.9:g.72814629C>G
NCBI36
Search 100 bp 5'
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