Canonical Allele Identifier: CA607341396
Gene: LINC02356 HGNC NCBI

Linked Data

dbSNP Id: rs1342777703
gnomAD v2: 12-111836916-C-T
gnomAD v3: 12-111399112-C-T
gnomAD v4: 12-111399112-C-T
MyVariant Identifiers: chr12:g.111836916C>T (hg19) chr12:g.111399112C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111399112C>T , CM000674.2:g.111399112C>T GRCh38
NC_000012.11:g.111836916C>T , CM000674.1:g.111836916C>T GRCh37
NC_000012.10:g.110321299C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945342.1:n.44+2239C>T
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