ClinGen Allele Registry
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Canonical Allele Identifier:
CA557734261
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.4196292_4196293delinsGT
GRCh37
chr5:g.4196405_4196406delinsGT
Linked Data - Sequence & Population
gnomAD v2:
5:4196405 A / G
gnomAD v3:
5:4196292 A / G
gnomAD v4:
chr5-4196292-A-G
Linked Data - NCBI & NCI
dbSNP:
1561024780
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.4196292A>G , CM000667.2:g.4196292A>G
GRCh38
NC_000005.9:g.4196405A>G , CM000667.1:g.4196405A>G
GRCh37
NC_000005.8:g.4249405A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'