Canonical Allele Identifier: CA1693197804
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs1562626540

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20845398G>C , CM000669.2:g.20845398G>C GRCh38
NC_000007.13:g.20885017G>C , CM000669.1:g.20885017G>C GRCh37
NC_000007.12:g.20851542G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.74+9894G>C