Canonical Allele Identifier: CA1127548456
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs1827341238

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261884_103261885del , CM000671.2:g.103261884_103261885del GRCh38
NC_000009.11:g.106024166_106024167del , CM000671.1:g.106024166_106024167del GRCh37
NC_000009.10:g.105063987_105063988del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2642_771+2643del