Canonical Allele Identifier: CA1276001839
Gene: LINC01965 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103962166T= , CM000664.2:g.103962166T= GRCh38
NC_000002.11:g.104578624T= , CM000664.1:g.104578624T= GRCh37
NC_000002.10:g.103945056T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739621.1:n.178+87721T=
XR_001739623.1:n.178+87721T=