ClinGen Allele Registry
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Canonical Allele Identifier:
CA595448893
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.99781726C>T
GRCh37
chr10:g.101541483C>T
Linked Data - Sequence & Population
gnomAD v2:
10:101541483 C / T
gnomAD v3:
10:99781726 C / T
gnomAD v4:
chr10-99781726-C-T
Linked Data - NCBI & NCI
dbSNP:
1333594294
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.99781726C>T , CM000672.2:g.99781726C>T
GRCh38
NC_000010.10:g.101541483C>T , CM000672.1:g.101541483C>T
GRCh37
NC_000010.9:g.101531473C>T
NCBI36
NG_011798.1:g.4021C>T
NG_011798.2:g.4129C>T
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