Canonical Allele Identifier: CA627574244
Gene: LINC00469 HGNC NCBI

Linked Data

dbSNP Id: rs1168636557
gnomAD v2: 17-71807528-AT-A
gnomAD v3: 17-73811389-AT-A
gnomAD v4: 17-73811389-AT-A
MyVariant Identifiers: chr17:g.71807529del (hg19) chr17:g.73811390del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811394del , CM000679.2:g.73811394del GRCh38
NC_000017.10:g.71807533del , CM000679.1:g.71807533del GRCh37
NC_000017.9:g.69319128del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027146.1:n.228+12298del
Search 100 bp 5'
Search 100 bp 3'