Canonical Allele Identifier: CA673995864

Gene: LINC02751

Linked Data

• dbSNP Id: rs1312123548
• gnomAD v3: 11-15598983-A-G
• gnomAD v4: 11-15598983-A-G
• MyVariant Identifiers: chr11:g.15620529A>G (hg19) ; chr11:g.15598983A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.15598983A>G , CM000673.2:g.15598983A>G	GRCh38
NC_000011.9:g.15620529A>G , CM000673.1:g.15620529A>G	GRCh37
NC_000011.8:g.15577105A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_931072.1:n.445-9733T>C
XR_931073.1:n.444-9733T>C
XR_931074.1:n.445-13692T>C
XR_931075.1:n.444+23322T>C
XR_931076.1:n.169-4949A>G
XR_931077.1:n.443-4949A>G
XR_931072.3:n.445-9733T>C
XR_931075.2:n.444+23322T>C
XR_931076.3:n.506-4949A>G
NR_169502.1:n.587+13181A>G
NR_169503.1:n.505+13181A>G
NR_169504.1:n.506-4949A>G
NR_169505.1:n.506-3719A>G
NR_169506.1:n.1097-3719A>G