Canonical Allele Identifier: CA596504181
Gene: LINC01153 HGNC NCBI

Linked Data

dbSNP Id: rs1475039428
gnomAD v2: 10-122939316-GA-G
gnomAD v3: 10-121179802-GA-G
gnomAD v4: 10-121179802-GA-G
MyVariant Identifiers: chr10:g.122939317del (hg19) chr10:g.121179803del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121179803del , CM000672.2:g.121179803del GRCh38
NC_000010.10:g.122939317del , CM000672.1:g.122939317del GRCh37
NC_000010.9:g.122929307del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_246197.2:n.684+831del
Search 100 bp 5'
Search 100 bp 3'