Canonical Allele Identifier: CA1356515767
Gene: LINC01811 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.34170674T= , CM000665.2:g.34170674T= GRCh38
NC_000003.11:g.34212166T= , CM000665.1:g.34212166T= GRCh37
NC_000003.10:g.34187170T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245201.3:n.110-171T=
XR_940705.1:n.110-171T=
XR_940707.1:n.80-171T=
XR_940708.1:n.76-171T=
XR_001740638.1:n.59-171T=
XR_001740639.1:n.272-171T=
XR_002959622.1:n.68-171T=
XR_002959623.1:n.272-171T=