Canonical Allele Identifier: CA951840648

Gene: LINC02356

Linked Data

• dbSNP Id: rs1869953323
• gnomAD v3: 12-111399116-GTC-G
• gnomAD v4: 12-111399116-GTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111399121_111399122del , CM000674.2:g.111399121_111399122del	GRCh38
NC_000012.11:g.111836925_111836926del , CM000674.1:g.111836925_111836926del	GRCh37
NC_000012.10:g.110321308_110321309del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_945342.1:n.44+2248_44+2249del