Canonical Allele Identifier: CA185516667
Gene: LINC02964 HGNC NCBI

Linked Data

dbSNP Id: rs568632900

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527820T>A , CM000670.2:g.125527820T>A GRCh38
NC_000008.10:g.126540062T>A , CM000670.1:g.126540062T>A GRCh37
NC_000008.9:g.126609244T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928628.1:n.256+54506T>A
XR_001746072.1:n.583+4807T>A
XR_001746073.1:n.583+4807T>A