Canonical Allele Identifier: CA86469744

Gene: LINC00880

Linked Data

• dbSNP Id: rs1000349801
• gnomAD v2: 3-156836960-A-G
• gnomAD v3: 3-157119171-A-G
• gnomAD v4: 3-157119171-A-G
• MyVariant Identifiers: chr3:g.156836960A>G (hg19) ; chr3:g.157119171A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.157119171A>G , CM000665.2:g.157119171A>G	GRCh38
NC_000003.11:g.156836960A>G , CM000665.1:g.156836960A>G	GRCh37
NC_000003.10:g.158319654A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_034007.1:n.127+3705T>C