Canonical Allele Identifier: CA1055324337

Gene: LINC00880

Linked Data

• dbSNP Id: rs1737283532
• gnomAD v3: 3-157119211-A-T
• gnomAD v4: 3-157119211-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.157119211A>T , CM000665.2:g.157119211A>T	GRCh38
NC_000003.11:g.156837000A>T , CM000665.1:g.156837000A>T	GRCh37
NC_000003.10:g.158319694A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_034007.1:n.127+3665T>A