Canonical Allele Identifier: CA13925861
Gene: LINC02334 HGNC NCBI

Linked Data

dbSNP Id: rs9548119

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.37957444T>A , CM000675.2:g.37957444T>A GRCh38
NC_000013.10:g.38531581T>A , CM000675.1:g.38531581T>A GRCh37
NC_000013.9:g.37429581T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941877.1:n.466+22407T>A
XR_941878.1:n.466+22407T>A
XR_941879.1:n.466+22407T>A
XR_941880.1:n.466+22407T>A
XR_941881.1:n.466+22407T>A
XR_941882.1:n.325+22548T>A
XR_941877.2:n.536+22407T>A
XR_941880.3:n.539+22407T>A