Canonical Allele Identifier: CA1954304038
Gene: LINC02751 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.15598957A= , CM000673.2:g.15598957A= GRCh38
NC_000011.9:g.15620503A= , CM000673.1:g.15620503A= GRCh37
NC_000011.8:g.15577079A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_931072.1:n.445-9707T=
XR_931073.1:n.444-9707T=
XR_931074.1:n.445-13666T=
XR_931075.1:n.444+23348T=
XR_931076.1:n.169-4975A=
XR_931077.1:n.443-4975A=
XR_931072.3:n.445-9707T=
XR_931075.2:n.444+23348T=
XR_931076.3:n.506-4975A=
NR_169502.1:n.587+13155A=
NR_169503.1:n.505+13155A=
NR_169504.1:n.506-4975A=
NR_169505.1:n.506-3745A=
NR_169506.1:n.1097-3745A=