Canonical Allele Identifier: CA951840624
Gene: LINC02356 HGNC NCBI

Linked Data

dbSNP Id: rs550255502
gnomAD v3: 12-111398974-C-T
gnomAD v4: 12-111398974-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111398974C>T , CM000674.2:g.111398974C>T GRCh38
NC_000012.11:g.111836778C>T , CM000674.1:g.111836778C>T GRCh37
NC_000012.10:g.110321161C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945342.1:n.44+2101C>T
Search 100 bp 5'
Search 100 bp 3'