Canonical Allele Identifier: CA1817470565
Gene: LINC02964 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527730T= , CM000670.2:g.125527730T= GRCh38
NC_000008.10:g.126539972T= , CM000670.1:g.126539972T= GRCh37
NC_000008.9:g.126609154T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928628.1:n.256+54416T=
XR_001746072.1:n.583+4717T=
XR_001746073.1:n.583+4717T=