Canonical Allele Identifier: CA774933186

Gene: LINC00469

Linked Data

• dbSNP Id: rs1205406135
• gnomAD v3: 17-73811576-C-T
• gnomAD v4: 17-73811576-C-T
• MyVariant Identifiers: chr17:g.71807715C>T (hg19) ; chr17:g.73811576C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.73811576C>T , CM000679.2:g.73811576C>T	GRCh38
NC_000017.10:g.71807715C>T , CM000679.1:g.71807715C>T	GRCh37
NC_000017.9:g.69319310C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_027146.1:n.228+12112G>A