ClinGen Allele Registry
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Canonical Allele Identifier:
CA112916488
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.1296373G>C
GRCh37
chr5:g.1296488G>C
Linked Data - Sequence & Population
gnomAD v3:
5:1296373 G / C
gnomAD v4:
chr5-1296373-G-C
Linked Data - NCBI & NCI
dbSNP:
922163867
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.1296373G>C , CM000667.2:g.1296373G>C
GRCh38
NC_000005.9:g.1296488G>C , CM000667.1:g.1296488G>C
GRCh37
NC_000005.8:g.1349488G>C
NCBI36
NG_009265.1:g.3675C>G , LRG_343:g.3675C>G
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