Canonical Allele Identifier: CA1445661299
Gene: LINC02357 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083896G= , CM000666.2:g.26083896G= GRCh38
NC_000004.11:g.26085518G= , CM000666.1:g.26085518G= GRCh37
NC_000004.10:g.25694616G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3306G=
XR_925506.3:n.1408+3306G=