Canonical Allele Identifier: CA294608031

Gene: LINC00469

Linked Data

• dbSNP Id: rs906446616
• gnomAD v2: 17-71807730-C-T
• gnomAD v3: 17-73811591-C-T
• gnomAD v4: 17-73811591-C-T
• MyVariant Identifiers: chr17:g.71807730C>T (hg19) ; chr17:g.73811591C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.73811591C>T , CM000679.2:g.73811591C>T	GRCh38
NC_000017.10:g.71807730C>T , CM000679.1:g.71807730C>T	GRCh37
NC_000017.9:g.69319325C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_027146.1:n.228+12097G>A