Canonical Allele Identifier: CA1276001743
Gene: LINC01965 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103961931G= , CM000664.2:g.103961931G= GRCh38
NC_000002.11:g.104578389G= , CM000664.1:g.104578389G= GRCh37
NC_000002.10:g.103944821G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739621.1:n.178+87486G=
XR_001739623.1:n.178+87486G=