Canonical Allele Identifier: CA2713886998
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs1783252953

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954773G>T , CM000669.2:g.20954773G>T GRCh38
NC_000007.13:g.20994392G>T , CM000669.1:g.20994392G>T GRCh37
NC_000007.12:g.20960917G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.152-66095G>T