Canonical Allele Identifier: CA1445661261
Gene: LINC02357 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083868T= , CM000666.2:g.26083868T= GRCh38
NC_000004.11:g.26085490T= , CM000666.1:g.26085490T= GRCh37
NC_000004.10:g.25694588T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3278T=
XR_925506.3:n.1408+3278T=