Canonical Allele Identifier: CA607341394
Gene: LINC02356 HGNC NCBI

Linked Data

dbSNP Id: rs1234718330
gnomAD v2: 12-111836890-C-T
gnomAD v3: 12-111399086-C-T
gnomAD v4: 12-111399086-C-T
MyVariant Identifiers: chr12:g.111836890C>T (hg19) chr12:g.111399086C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111399086C>T , CM000674.2:g.111399086C>T GRCh38
NC_000012.11:g.111836890C>T , CM000674.1:g.111836890C>T GRCh37
NC_000012.10:g.110321273C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945342.1:n.44+2213C>T
Search 100 bp 5'
Search 100 bp 3'