Canonical Allele Identifier: CA955072001
Gene: LINC02334 HGNC NCBI

Linked Data

dbSNP Id: rs1869153334

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.37957451dup , CM000675.2:g.37957451dup GRCh38
NC_000013.10:g.38531588dup , CM000675.1:g.38531588dup GRCh37
NC_000013.9:g.37429588dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941877.1:n.466+22414dup
XR_941878.1:n.466+22414dup
XR_941879.1:n.466+22414dup
XR_941880.1:n.466+22414dup
XR_941881.1:n.466+22414dup
XR_941882.1:n.325+22555dup
XR_941877.2:n.536+22414dup
XR_941880.3:n.539+22414dup