Canonical Allele Identifier: CA1276001834
Gene: LINC01965 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103962147T= , CM000664.2:g.103962147T= GRCh38
NC_000002.11:g.104578605T= , CM000664.1:g.104578605T= GRCh37
NC_000002.10:g.103945037T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739621.1:n.178+87702T=
XR_001739623.1:n.178+87702T=