Canonical Allele Identifier: CA2751510125
Gene: LINC01965 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103962103G>T , CM000664.2:g.103962103G>T GRCh38
NC_000002.11:g.104578561G>T , CM000664.1:g.104578561G>T GRCh37
NC_000002.10:g.103944993G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739621.1:n.178+87658G>T
XR_001739623.1:n.178+87658G>T