Canonical Allele Identifier: CA1693197813
Gene: LINC01162 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20845411C= , CM000669.2:g.20845411C= GRCh38
NC_000007.13:g.20885030C= , CM000669.1:g.20885030C= GRCh37
NC_000007.12:g.20851555C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.74+9907C=