Canonical Allele Identifier: CA1954304057
Gene: LINC02751 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.15599017A= , CM000673.2:g.15599017A= GRCh38
NC_000011.9:g.15620563A= , CM000673.1:g.15620563A= GRCh37
NC_000011.8:g.15577139A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_931072.1:n.445-9767T=
XR_931073.1:n.444-9767T=
XR_931074.1:n.445-13726T=
XR_931075.1:n.444+23288T=
XR_931076.1:n.169-4915A=
XR_931077.1:n.443-4915A=
XR_931072.3:n.445-9767T=
XR_931075.2:n.444+23288T=
XR_931076.3:n.506-4915A=
NR_169502.1:n.587+13215A=
NR_169503.1:n.505+13215A=
NR_169504.1:n.506-4915A=
NR_169505.1:n.506-3685A=
NR_169506.1:n.1097-3685A=