Canonical Allele Identifier: CA1445661326
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs970357905

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083919G>A , CM000666.2:g.26083919G>A GRCh38
NC_000004.11:g.26085541G>A , CM000666.1:g.26085541G>A GRCh37
NC_000004.10:g.25694639G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925506.1:n.1401+3329G>A
XR_925506.3:n.1408+3329G>A