Canonical Allele Identifier: CA1445661320
Gene: LINC02357 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083910G= , CM000666.2:g.26083910G= GRCh38
NC_000004.11:g.26085532G= , CM000666.1:g.26085532G= GRCh37
NC_000004.10:g.25694630G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3320G=
XR_925506.3:n.1408+3320G=