Canonical Allele Identifier: CA1817470520
Gene: LINC02964 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527639C= , CM000670.2:g.125527639C= GRCh38
NC_000008.10:g.126539881C= , CM000670.1:g.126539881C= GRCh37
NC_000008.9:g.126609063C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928628.1:n.256+54325C=
XR_001746072.1:n.583+4626C=
XR_001746073.1:n.583+4626C=