Canonical Allele Identifier: CA1693234882
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs1783254415

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954906C>T , CM000669.2:g.20954906C>T GRCh38
NC_000007.13:g.20994525C>T , CM000669.1:g.20994525C>T GRCh37
NC_000007.12:g.20961050C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.152-65962C>T