Canonical Allele Identifier: CA1276001829
Gene: LINC01965 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103962138G= , CM000664.2:g.103962138G= GRCh38
NC_000002.11:g.104578596G= , CM000664.1:g.104578596G= GRCh37
NC_000002.10:g.103945028G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739621.1:n.178+87693G=
XR_001739623.1:n.178+87693G=