Canonical Allele Identifier: CA2760799680
Gene: LINC02357 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083932G>A , CM000666.2:g.26083932G>A GRCh38
NC_000004.11:g.26085554G>A , CM000666.1:g.26085554G>A GRCh37
NC_000004.10:g.25694652G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3342G>A
XR_925506.3:n.1408+3342G>A