Canonical Allele Identifier: CA294608033

Gene: LINC00469

Linked Data

• dbSNP Id: rs999421795
• gnomAD v2: 17-71807732-T-C
• gnomAD v3: 17-73811593-T-C
• gnomAD v4: 17-73811593-T-C
• MyVariant Identifiers: chr17:g.71807732T>C (hg19) ; chr17:g.73811593T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.73811593T>C , CM000679.2:g.73811593T>C	GRCh38
NC_000017.10:g.71807732T>C , CM000679.1:g.71807732T>C	GRCh37
NC_000017.9:g.69319327T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_027146.1:n.228+12095A>G