Canonical Allele Identifier: CA1869205489
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs1827343053

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103262014_103262019del , CM000671.2:g.103262014_103262019del GRCh38
NC_000009.11:g.106024296_106024301del , CM000671.1:g.106024296_106024301del GRCh37
NC_000009.10:g.105064117_105064122del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2507_771+2512del