Canonical Allele Identifier: CA197961792
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs977643032

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261879_103261883del , CM000671.2:g.103261879_103261883del GRCh38
NC_000009.11:g.106024161_106024165del , CM000671.1:g.106024161_106024165del GRCh37
NC_000009.10:g.105063982_105063986del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121578.1:n.771+2647_771+2651del