Canonical Allele Identifier: CA1445661337
Gene: LINC02357 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083928C= , CM000666.2:g.26083928C= GRCh38
NC_000004.11:g.26085550C= , CM000666.1:g.26085550C= GRCh37
NC_000004.10:g.25694648C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3338C=
XR_925506.3:n.1408+3338C=