Canonical Allele Identifier: CA1445661199
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs1714635049

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083804del , CM000666.2:g.26083804del GRCh38
NC_000004.11:g.26085426del , CM000666.1:g.26085426del GRCh37
NC_000004.10:g.25694524del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3214del
XR_925506.3:n.1408+3214del