Canonical Allele Identifier: CA197961773
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs779370140
MyVariant Identifiers: chr9:g.106024097_106024098del (hg19) chr9:g.103261815_103261816del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261817_103261818del , CM000671.2:g.103261817_103261818del GRCh38
NC_000009.11:g.106024099_106024100del , CM000671.1:g.106024099_106024100del GRCh37
NC_000009.10:g.105063920_105063921del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2708_771+2709del
Search 100 bp 5'
Search 100 bp 3'