ClinGen Allele Registry
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Canonical Allele Identifier:
CA557546666
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.1296298A>G
GRCh37
chr5:g.1296413A>G
Linked Data - Sequence & Population
gnomAD v2:
5:1296413 A / G
gnomAD v3:
5:1296298 A / G
gnomAD v4:
chr5-1296298-A-G
Linked Data - NCBI & NCI
dbSNP:
1351887977
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.1296298A>G , CM000667.2:g.1296298A>G
GRCh38
NC_000005.9:g.1296413A>G , CM000667.1:g.1296413A>G
GRCh37
NC_000005.8:g.1349413A>G
NCBI36
NG_009265.1:g.3750T>C , LRG_343:g.3750T>C
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