Canonical Allele Identifier: CA1445661256
Gene: LINC02357 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083866T= , CM000666.2:g.26083866T= GRCh38
NC_000004.11:g.26085488T= , CM000666.1:g.26085488T= GRCh37
NC_000004.10:g.25694586T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3276T=
XR_925506.3:n.1408+3276T=