Canonical Allele Identifier: CA1693197835
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs1781823052

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20845426C>A , CM000669.2:g.20845426C>A GRCh38
NC_000007.13:g.20885045C>A , CM000669.1:g.20885045C>A GRCh37
NC_000007.12:g.20851570C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.74+9922C>A