Canonical Allele Identifier: CA1693234801
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs1783253742

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954840T>C , CM000669.2:g.20954840T>C GRCh38
NC_000007.13:g.20994459T>C , CM000669.1:g.20994459T>C GRCh37
NC_000007.12:g.20960984T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.152-66028T>C