Canonical Allele Identifier: CA294608032

Gene: LINC00469

Linked Data

• dbSNP Id: rs1021372122
• gnomAD v3: 17-73811592-G-A
• gnomAD v4: 17-73811592-G-A
• MyVariant Identifiers: chr17:g.71807731G>A (hg19) ; chr17:g.73811592G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.73811592G>A , CM000679.2:g.73811592G>A	GRCh38
NC_000017.10:g.71807731G>A , CM000679.1:g.71807731G>A	GRCh37
NC_000017.9:g.69319326G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_027146.1:n.228+12096C>T