Canonical Allele Identifier: CA1055324221

Gene: LINC00880

Linked Data

• dbSNP Id: rs1737281028
• gnomAD v3: 3-157119057-T-A
• gnomAD v4: 3-157119057-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.157119057T>A , CM000665.2:g.157119057T>A	GRCh38
NC_000003.11:g.156836846T>A , CM000665.1:g.156836846T>A	GRCh37
NC_000003.10:g.158319540T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_034007.1:n.127+3819A>T