Canonical Allele Identifier: CA1055324333

Gene: LINC00880

Linked Data

• dbSNP Id: rs1737283451
• gnomAD v3: 3-157119208-A-G
• gnomAD v4: 3-157119208-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.157119208A>G , CM000665.2:g.157119208A>G	GRCh38
NC_000003.11:g.156836997A>G , CM000665.1:g.156836997A>G	GRCh37
NC_000003.10:g.158319691A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_034007.1:n.127+3668T>C