Canonical Allele Identifier: CA1276001851
Gene: LINC01965 HGNC NCBI

Linked Data

dbSNP Id: rs1680652234

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.103962191_103962195del , CM000664.2:g.103962191_103962195del GRCh38
NC_000002.11:g.104578649_104578653del , CM000664.1:g.104578649_104578653del GRCh37
NC_000002.10:g.103945081_103945085del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739621.1:n.178+87746_178+87750del
XR_001739623.1:n.178+87746_178+87750del