Canonical Allele Identifier: CA1693234851
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs1783254073

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954880T>C , CM000669.2:g.20954880T>C GRCh38
NC_000007.13:g.20994499T>C , CM000669.1:g.20994499T>C GRCh37
NC_000007.12:g.20961024T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.152-65988T>C