Canonical Allele Identifier: CA218285032

Gene: LINC02751

Linked Data

• dbSNP Id: rs1020194720
• MyVariant Identifiers: chr11:g.15620534_15620535insTT (hg19) ; chr11:g.15598988_15598989insTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.15598989_15598990insTT , CM000673.2:g.15598989_15598990insTT	GRCh38
NC_000011.9:g.15620535_15620536insTT , CM000673.1:g.15620535_15620536insTT	GRCh37
NC_000011.8:g.15577111_15577112insTT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_931072.1:n.445-9739_445-9738insAA
XR_931073.1:n.444-9739_444-9738insAA
XR_931074.1:n.445-13698_445-13697insAA
XR_931075.1:n.444+23316_444+23317insAA
XR_931076.1:n.169-4943_169-4942insTT
XR_931077.1:n.443-4943_443-4942insTT
XR_931072.3:n.445-9739_445-9738insAA
XR_931075.2:n.444+23316_444+23317insAA
XR_931076.3:n.506-4943_506-4942insTT
NR_169502.1:n.587+13187_587+13188insTT
NR_169503.1:n.505+13187_505+13188insTT
NR_169504.1:n.506-4943_506-4942insTT
NR_169505.1:n.506-3713_506-3712insTT
NR_169506.1:n.1097-3713_1097-3712insTT