ClinGen Allele Registry
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Canonical Allele Identifier:
CA786414637
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.122589870_122589871insT
GRCh37
chr4:g.123511025_123511026insT
Linked Data - Sequence & Population
gnomAD v3:
4:122589870 C / CT
gnomAD v4:
chr4-122589870-C-CT
Linked Data - NCBI & NCI
dbSNP:
1295256239
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.122589871dup , CM000666.2:g.122589871dup
GRCh38
NC_000004.11:g.123511026dup , CM000666.1:g.123511026dup
GRCh37
NC_000004.10:g.123730476dup
NCBI36
Search 100 bp 5'
Search 100 bp 3'