ClinGen Allele Registry
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Canonical Allele Identifier:
CA124378727
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.104872224A>G
GRCh37
chr5:g.104207925A>G
Linked Data - Sequence & Population
gnomAD v3:
5:104872224 A / G
gnomAD v4:
chr5-104872224-A-G
Linked Data - NCBI & NCI
dbSNP:
1019109015
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.104872224A>G , CM000667.2:g.104872224A>G
GRCh38
NC_000005.9:g.104207925A>G , CM000667.1:g.104207925A>G
GRCh37
NC_000005.8:g.104235824A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'