Canonical Allele Identifier: CA1055324270

Gene: LINC00880

Linked Data

• dbSNP Id: rs1737283118
• gnomAD v3: 3-157119173-G-A
• gnomAD v4: 3-157119173-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.157119173G>A , CM000665.2:g.157119173G>A	GRCh38
NC_000003.11:g.156836962G>A , CM000665.1:g.156836962G>A	GRCh37
NC_000003.10:g.158319656G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_034007.1:n.127+3703C>T