ClinGen Allele Registry
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Canonical Allele Identifier:
CA129850813
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.159387430C>G
Linked Data - Sequence & Population
gnomAD v3:
5:159387430 C / G
gnomAD v4:
chr5-159387430-C-G
Linked Data - NCBI & NCI
dbSNP:
1027566431
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.159387430C>G , CM000667.2:g.159387430C>G
GRCh38
NC_000005.9:g.158814438C>G , CM000667.1:g.158814438C>G
GRCh37
NC_000005.8:g.158747016C>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'