Canonical Allele Identifier: CA1817470599
Gene: LINC02964 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527822C= , CM000670.2:g.125527822C= GRCh38
NC_000008.10:g.126540064C= , CM000670.1:g.126540064C= GRCh37
NC_000008.9:g.126609246C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928628.1:n.256+54508C=
XR_001746072.1:n.583+4809C=
XR_001746073.1:n.583+4809C=