Canonical Allele Identifier: CA2514174614
Gene: LINC01162 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954916T>A , CM000669.2:g.20954916T>A GRCh38
NC_000007.13:g.20994535T>A , CM000669.1:g.20994535T>A GRCh37
NC_000007.12:g.20961060T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.152-65952T>A