Canonical Allele Identifier: CA2063275136
Gene: LINC02356 HGNC NCBI

Linked Data

dbSNP Id: rs1593017766
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111399116G>T , CM000674.2:g.111399116G>T GRCh38
NC_000012.11:g.111836920G>T , CM000674.1:g.111836920G>T GRCh37
NC_000012.10:g.110321303G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945342.1:n.44+2243G>T
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Search 100 bp 3'