Canonical Allele Identifier: CA1693197786
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs1781822624

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20845379_20845389del , CM000669.2:g.20845379_20845389del GRCh38
NC_000007.13:g.20884998_20885008del , CM000669.1:g.20884998_20885008del GRCh37
NC_000007.12:g.20851523_20851533del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.74+9875_74+9885del