ClinGen Allele Registry
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Canonical Allele Identifier:
CA596265797
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.117586460G>T
GRCh37
chr10:g.119345971G>T
Linked Data - Sequence & Population
gnomAD v2:
10:119345971 G / T
gnomAD v3:
10:117586460 G / T
gnomAD v4:
chr10-117586460-G-T
Linked Data - NCBI & NCI
dbSNP:
1450715959
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.117586460G>T , CM000672.2:g.117586460G>T
GRCh38
NC_000010.10:g.119345971G>T , CM000672.1:g.119345971G>T
GRCh37
NC_000010.9:g.119335961G>T
NCBI36
Search 100 bp 5'
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