Canonical Allele Identifier: CA862161286
Gene:

Linked Data

dbSNP Id: rs1244347322
gnomAD v3: 9-21755978-AC-A
gnomAD v4: 9-21755978-AC-A
MyVariant Identifiers: chr9:g.21755978del (hg19) chr9:g.21755979del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21755979del , CM000671.2:g.21755979del GRCh38
NC_000009.11:g.21755978del , CM000671.1:g.21755978del GRCh37
NC_000009.10:g.21745978del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746563.2:n.163+11846del
Search 100 bp 5'
Search 100 bp 3'