Canonical Allele Identifier: CA2760799681
Gene: LINC02357 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083943G>T , CM000666.2:g.26083943G>T GRCh38
NC_000004.11:g.26085565G>T , CM000666.1:g.26085565G>T GRCh37
NC_000004.10:g.25694663G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3353G>T
XR_925506.3:n.1408+3353G>T