Canonical Allele Identifier: CA2700114821
Gene: LINC01965 HGNC NCBI

Linked Data

dbSNP Id: rs1416761405

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103962125G>T , CM000664.2:g.103962125G>T GRCh38
NC_000002.11:g.104578583G>T , CM000664.1:g.104578583G>T GRCh37
NC_000002.10:g.103945015G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739621.1:n.178+87680G>T
XR_001739623.1:n.178+87680G>T