Canonical Allele Identifier: CA651654572
Gene: LINC01162 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954775T>A , CM000669.2:g.20954775T>A GRCh38
NC_000007.13:g.20994394T>A , CM000669.1:g.20994394T>A GRCh37
NC_000007.12:g.20960919T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_126381.1:n.152-66093T>A