Canonical Allele Identifier: CA1445661271
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs1714636975

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083876_26083877insCC , CM000666.2:g.26083876_26083877insCC GRCh38
NC_000004.11:g.26085498_26085499insCC , CM000666.1:g.26085498_26085499insCC GRCh37
NC_000004.10:g.25694596_25694597insCC NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3286_1401+3287insCC
XR_925506.3:n.1408+3286_1408+3287insCC