Canonical Allele Identifier: CA589962201
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs1234905314

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261877_103261880del , CM000671.2:g.103261877_103261880del GRCh38
NC_000009.11:g.106024159_106024162del , CM000671.1:g.106024159_106024162del GRCh37
NC_000009.10:g.105063980_105063983del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121578.1:n.771+2647_771+2650del