Canonical Allele Identifier: CA1693197832
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs1781823029

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20845424C>G , CM000669.2:g.20845424C>G GRCh38
NC_000007.13:g.20885043C>G , CM000669.1:g.20885043C>G GRCh37
NC_000007.12:g.20851568C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.74+9920C>G