Canonical Allele Identifier: CA1817470553
Gene: LINC02964 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527708C= , CM000670.2:g.125527708C= GRCh38
NC_000008.10:g.126539950C= , CM000670.1:g.126539950C= GRCh37
NC_000008.9:g.126609132C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928628.1:n.256+54394C=
XR_001746072.1:n.583+4695C=
XR_001746073.1:n.583+4695C=