Canonical Allele Identifier: CA86469740

Gene: LINC00880

Linked Data

• dbSNP Id: rs527637257
• gnomAD v3: 3-157119115-C-T
• gnomAD v4: 3-157119115-C-T
• MyVariant Identifiers: chr3:g.156836904C>T (hg19) ; chr3:g.157119115C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.157119115C>T , CM000665.2:g.157119115C>T	GRCh38
NC_000003.11:g.156836904C>T , CM000665.1:g.156836904C>T	GRCh37
NC_000003.10:g.158319598C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_034007.1:n.127+3761G>A