Canonical Allele Identifier: CA1693234781
Gene: LINC01162 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954825T= , CM000669.2:g.20954825T= GRCh38
NC_000007.13:g.20994444T= , CM000669.1:g.20994444T= GRCh37
NC_000007.12:g.20960969T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.152-66043T=