Canonical Allele Identifier: CA2104288175

Gene: LINC00331

Linked Data

• dbSNP Id: rs1880407819

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.78836475_78836476insC , CM000675.2:g.78836475_78836476insC	GRCh38
NC_000013.10:g.79410610_79410611insC , CM000675.1:g.79410610_79410611insC	GRCh37
NC_000013.9:g.78308611_78308612insC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046869.2:n.111+3464_111+3465insG