Canonical Allele Identifier: CA11366447
Gene: LINC00877 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.72091381G>A , CM000665.2:g.72091381G>A GRCh38
NC_000003.11:g.72140532G>A , CM000665.1:g.72140532G>A GRCh37
NC_000003.10:g.72223222G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104116.1:n.394+8523C>T
Search 100 bp 5'
Search 100 bp 3'