Canonical Allele Identifier: CA1445661242
Gene: LINC02357 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083855T= , CM000666.2:g.26083855T= GRCh38
NC_000004.11:g.26085477T= , CM000666.1:g.26085477T= GRCh37
NC_000004.10:g.25694575T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925506.1:n.1401+3265T=
XR_925506.3:n.1408+3265T=