Canonical Allele Identifier: CA857924200
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs1372342826

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261994del , CM000671.2:g.103261994del GRCh38
NC_000009.11:g.106024276del , CM000671.1:g.106024276del GRCh37
NC_000009.10:g.105064097del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121578.1:n.771+2530del