Canonical Allele Identifier: CA1693234891
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs1783254498

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954912C>A , CM000669.2:g.20954912C>A GRCh38
NC_000007.13:g.20994531C>A , CM000669.1:g.20994531C>A GRCh37
NC_000007.12:g.20961056C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.152-65956C>A