Canonical Allele Identifier: CA1276001732
Gene: LINC01965 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103961910G= , CM000664.2:g.103961910G= GRCh38
NC_000002.11:g.104578368G= , CM000664.1:g.104578368G= GRCh37
NC_000002.10:g.103944800G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739621.1:n.178+87465G=
XR_001739623.1:n.178+87465G=