Canonical Allele Identifier: CA1445661212
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs1714635326
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083820C>T , CM000666.2:g.26083820C>T GRCh38
NC_000004.11:g.26085442C>T , CM000666.1:g.26085442C>T GRCh37
NC_000004.10:g.25694540C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3230C>T
XR_925506.3:n.1408+3230C>T
Search 100 bp 5'
Search 100 bp 3'