Canonical Allele Identifier: CA1693197810
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs1583504773

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20845408T>C , CM000669.2:g.20845408T>C GRCh38
NC_000007.13:g.20885027T>C , CM000669.1:g.20885027T>C GRCh37
NC_000007.12:g.20851552T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.74+9904T>C