Canonical Allele Identifier: CA846958622
Gene: LINC02964 HGNC NCBI

Linked Data

dbSNP Id: rs1485326317

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527824_125527828del , CM000670.2:g.125527824_125527828del GRCh38
NC_000008.10:g.126540066_126540070del , CM000670.1:g.126540066_126540070del GRCh37
NC_000008.9:g.126609248_126609252del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928628.1:n.256+54510_256+54514del
XR_001746072.1:n.583+4811_583+4815del
XR_001746073.1:n.583+4811_583+4815del