Canonical Allele Identifier: CA1817470597
Gene: LINC02964 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527821G= , CM000670.2:g.125527821G= GRCh38
NC_000008.10:g.126540063G= , CM000670.1:g.126540063G= GRCh37
NC_000008.9:g.126609245G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928628.1:n.256+54507G=
XR_001746072.1:n.583+4808G=
XR_001746073.1:n.583+4808G=