Canonical Allele Identifier: CA15774356
Gene: LINC02341 HGNC NCBI

Linked Data

dbSNP Id: rs2062305

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.42478744G>A , CM000675.2:g.42478744G>A GRCh38
NC_000013.10:g.43052880G>A , CM000675.1:g.43052880G>A GRCh37
NC_000013.9:g.41950880G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941906.1:n.245-6725G>A
NR_135319.1:n.337-6725G>A