Canonical Allele Identifier: CA86469754

Gene: LINC00880

Linked Data

• dbSNP Id: rs971604327
• gnomAD v3: 3-157119326-G-A
• gnomAD v4: 3-157119326-G-A
• MyVariant Identifiers: chr3:g.156837115G>A (hg19) ; chr3:g.157119326G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.157119326G>A , CM000665.2:g.157119326G>A	GRCh38
NC_000003.11:g.156837115G>A , CM000665.1:g.156837115G>A	GRCh37
NC_000003.10:g.158319809G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_034007.1:n.127+3550C>T