Canonical Allele Identifier: CA1445661226
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs1714635622

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083845_26083873del , CM000666.2:g.26083845_26083873del GRCh38
NC_000004.11:g.26085467_26085495del , CM000666.1:g.26085467_26085495del GRCh37
NC_000004.10:g.25694565_25694593del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3255_1401+3283del
XR_925506.3:n.1408+3255_1408+3283del