Canonical Allele Identifier: CA1445661276
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs1714637072

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083881del , CM000666.2:g.26083881del GRCh38
NC_000004.11:g.26085503del , CM000666.1:g.26085503del GRCh37
NC_000004.10:g.25694601del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3291del
XR_925506.3:n.1408+3291del