Canonical Allele Identifier: CA754459859
Gene: LINC01965 HGNC NCBI

Linked Data

dbSNP Id: rs1222424910

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103962176del , CM000664.2:g.103962176del GRCh38
NC_000002.11:g.104578634del , CM000664.1:g.104578634del GRCh37
NC_000002.10:g.103945066del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739621.1:n.178+87731del
XR_001739623.1:n.178+87731del