Canonical Allele Identifier: CA1445661284
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs1714637093

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083883G>T , CM000666.2:g.26083883G>T GRCh38
NC_000004.11:g.26085505G>T , CM000666.1:g.26085505G>T GRCh37
NC_000004.10:g.25694603G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3293G>T
XR_925506.3:n.1408+3293G>T