Canonical Allele Identifier: CA1445661308
Gene: LINC02357 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083905T= , CM000666.2:g.26083905T= GRCh38
NC_000004.11:g.26085527T= , CM000666.1:g.26085527T= GRCh37
NC_000004.10:g.25694625T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3315T=
XR_925506.3:n.1408+3315T=