ClinGen Allele Registry
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Canonical Allele Identifier:
CA719894695
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.31096391C>T
GRCh37
chr16:g.31107712C>T
Linked Data - Sequence & Population
gnomAD v3:
16:31096391 C / T
gnomAD v4:
chr16-31096391-C-T
Linked Data - NCBI & NCI
dbSNP:
1192775936
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.31096391C>T , CM000678.2:g.31096391C>T
GRCh38
NC_000016.9:g.31107712C>T , CM000678.1:g.31107712C>T
GRCh37
NC_000016.8:g.31015213C>T
NCBI36
NG_011564.1:g.3565G>A
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