Canonical Allele Identifier: CA906518756
Gene: LINC01811 HGNC NCBI

Linked Data

dbSNP Id: rs6781182
MyVariant Identifiers: chr3:g.34212166T>A (hg19) chr3:g.34170674T>A (hg38)
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Genomic Alleles

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

Transcript Alleles

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