Canonical Allele Identifier: CA294608030

Gene: LINC00469

Linked Data

• dbSNP Id: rs892657250
• MyVariant Identifiers: chr17:g.71807720T>A (hg19) ; chr17:g.73811581T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.73811581T>A , CM000679.2:g.73811581T>A	GRCh38
NC_000017.10:g.71807720T>A , CM000679.1:g.71807720T>A	GRCh37
NC_000017.9:g.69319315T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_027146.1:n.228+12107A>T