Canonical Allele Identifier: CA1445661201
Gene: LINC02357 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083803C= , CM000666.2:g.26083803C= GRCh38
NC_000004.11:g.26085425C= , CM000666.1:g.26085425C= GRCh37
NC_000004.10:g.25694523C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3213C=
XR_925506.3:n.1408+3213C=