Canonical Allele Identifier: CA901232176

Gene: LINC00880

Linked Data

• dbSNP Id: rs900201814
• MyVariant Identifiers: chr3:g.156836920T>A (hg19) ; chr3:g.157119131T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.157119131T>A , CM000665.2:g.157119131T>A	GRCh38
NC_000003.11:g.156836920T>A , CM000665.1:g.156836920T>A	GRCh37
NC_000003.10:g.158319614T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_034007.1:n.127+3745A>T