Canonical Allele Identifier: CA1693197801
Gene: LINC01162 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20845396C= , CM000669.2:g.20845396C= GRCh38
NC_000007.13:g.20885015C= , CM000669.1:g.20885015C= GRCh37
NC_000007.12:g.20851540C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.74+9892C=