Canonical Allele Identifier: CA2727180374
Gene: LINC02356 HGNC NCBI

Linked Data

dbSNP Id: rs2135521912

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111398972_111398973insT , CM000674.2:g.111398972_111398973insT GRCh38
NC_000012.11:g.111836776_111836777insT , CM000674.1:g.111836776_111836777insT GRCh37
NC_000012.10:g.110321159_110321160insT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945342.1:n.44+2099_44+2100insT