Canonical Allele Identifier: CA1445661362
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs1714639083
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083967C>A , CM000666.2:g.26083967C>A GRCh38
NC_000004.11:g.26085589C>A , CM000666.1:g.26085589C>A GRCh37
NC_000004.10:g.25694687C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3377C>A
XR_925506.3:n.1408+3377C>A
Search 100 bp 5'
Search 100 bp 3'