Canonical Allele Identifier: CA1817470592
Gene: LINC02964 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527809G= , CM000670.2:g.125527809G= GRCh38
NC_000008.10:g.126540051G= , CM000670.1:g.126540051G= GRCh37
NC_000008.9:g.126609233G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928628.1:n.256+54495G=
XR_001746072.1:n.583+4796G=
XR_001746073.1:n.583+4796G=