Canonical Allele Identifier: CA243589033
Gene: LINC02356 HGNC NCBI

Linked Data

dbSNP Id: rs935366597
gnomAD v3: 12-111399068-T-A
gnomAD v4: 12-111399068-T-A
MyVariant Identifiers: chr12:g.111836872T>A (hg19) chr12:g.111399068T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111399068T>A , CM000674.2:g.111399068T>A GRCh38
NC_000012.11:g.111836872T>A , CM000674.1:g.111836872T>A GRCh37
NC_000012.10:g.110321255T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945342.1:n.44+2195T>A
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