Canonical Allele Identifier: CA2274723070

Gene: LINC00469

Linked Data

• dbSNP Id: rs2047487533

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.73811446C>T , CM000679.2:g.73811446C>T	GRCh38
NC_000017.10:g.71807585C>T , CM000679.1:g.71807585C>T	GRCh37
NC_000017.9:g.69319180C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_027146.1:n.228+12242G>A