Canonical Allele Identifier: CA1693197821
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs1781822968

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20845414T>C , CM000669.2:g.20845414T>C GRCh38
NC_000007.13:g.20885033T>C , CM000669.1:g.20885033T>C GRCh37
NC_000007.12:g.20851558T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.74+9910T>C