ClinGen Allele Registry
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Canonical Allele Identifier:
CA554476208
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.122590029_122590030insA
GRCh37
chr4:g.123511184_123511185insA
Linked Data - Sequence & Population
gnomAD v2:
4:123511184 T / TA
Linked Data - NCBI & NCI
dbSNP:
1377797566
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.122590030dup , CM000666.2:g.122590030dup
GRCh38
NC_000004.11:g.123511185dup , CM000666.1:g.123511185dup
GRCh37
NC_000004.10:g.123730635dup
NCBI36
Search 100 bp 5'
Search 100 bp 3'