Canonical Allele Identifier: CA1693234854
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs1783254100

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954881C>G , CM000669.2:g.20954881C>G GRCh38
NC_000007.13:g.20994500C>G , CM000669.1:g.20994500C>G GRCh37
NC_000007.12:g.20961025C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.152-65987C>G