Canonical Allele Identifier: CA294608046

Gene: LINC00469

Linked Data

• dbSNP Id: rs910143415
• MyVariant Identifiers: chr17:g.71807812G>A (hg19) ; chr17:g.73811673G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.73811673G>A , CM000679.2:g.73811673G>A	GRCh38
NC_000017.10:g.71807812G>A , CM000679.1:g.71807812G>A	GRCh37
NC_000017.9:g.69319407G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_027146.1:n.228+12015C>T