Canonical Allele Identifier: CA2714036973
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs2128086440

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954875A>C , CM000669.2:g.20954875A>C GRCh38
NC_000007.13:g.20994494A>C , CM000669.1:g.20994494A>C GRCh37
NC_000007.12:g.20961019A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.152-65993A>C