ClinGen Allele Registry
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Canonical Allele Identifier:
CA105250883
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.122759912del
GRCh37
chr4:g.123681067del
Linked Data - Sequence & Population
gnomAD v2:
4:123681066 TC / T
gnomAD v3:
4:122759911 TC / T
gnomAD v4:
chr4-122759911-TC-T
Linked Data - NCBI & NCI
dbSNP:
775326914
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.122759914del , CM000666.2:g.122759914del
GRCh38
NC_000004.11:g.123681069del , CM000666.1:g.123681069del
GRCh37
NC_000004.10:g.123900519del
NCBI36
Search 100 bp 5'
Search 100 bp 3'