Canonical Allele Identifier: CA1445661315
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs1714637776

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083906_26083915del , CM000666.2:g.26083906_26083915del GRCh38
NC_000004.11:g.26085528_26085537del , CM000666.1:g.26085528_26085537del GRCh37
NC_000004.10:g.25694626_25694635del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3316_1401+3325del
XR_925506.3:n.1408+3316_1408+3325del