Canonical Allele Identifier: CA774933086

Gene: LINC00469

Linked Data

• dbSNP Id: rs1363454959
• gnomAD v3: 17-73811455-G-T
• gnomAD v4: 17-73811455-G-T
• MyVariant Identifiers: chr17:g.71807594G>T (hg19) ; chr17:g.73811455G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.73811455G>T , CM000679.2:g.73811455G>T	GRCh38
NC_000017.10:g.71807594G>T , CM000679.1:g.71807594G>T	GRCh37
NC_000017.9:g.69319189G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_027146.1:n.228+12233C>A