ClinGen Allele Registry
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Canonical Allele Identifier:
CA557546665
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.1296281A>T
GRCh37
chr5:g.1296396A>T
Linked Data - Sequence & Population
gnomAD v2:
5:1296396 A / T
gnomAD v3:
5:1296281 A / T
gnomAD v4:
chr5-1296281-A-T
Linked Data - NCBI & NCI
dbSNP:
1262963388
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.1296281A>T , CM000667.2:g.1296281A>T
GRCh38
NC_000005.9:g.1296396A>T , CM000667.1:g.1296396A>T
GRCh37
NC_000005.8:g.1349396A>T
NCBI36
NG_009265.1:g.3767T>A , LRG_343:g.3767T>A
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