Canonical Allele Identifier: CA1693234842
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs12155172

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954872A>T , CM000669.2:g.20954872A>T GRCh38
NC_000007.13:g.20994491A>T , CM000669.1:g.20994491A>T GRCh37
NC_000007.12:g.20961016A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_126381.1:n.152-65996A>T