Canonical Allele Identifier: CA683615331
Gene: LINC02356 HGNC NCBI

Linked Data

dbSNP Id: rs1185771360
gnomAD v3: 12-111399089-G-T
gnomAD v4: 12-111399089-G-T
MyVariant Identifiers: chr12:g.111836893G>T (hg19) chr12:g.111399089G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111399089G>T , CM000674.2:g.111399089G>T GRCh38
NC_000012.11:g.111836893G>T , CM000674.1:g.111836893G>T GRCh37
NC_000012.10:g.110321276G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945342.1:n.44+2216G>T
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