Canonical Allele Identifier: CA16545526

Gene: LINC00469

Linked Data

• dbSNP Id: rs12451840
• gnomAD v2: 17-71807713-T-C
• gnomAD v3: 17-73811574-T-C
• gnomAD v4: 17-73811574-T-C
• MyVariant Identifiers: chr17:g.71807713T>C (hg19) ; chr17:g.73811574T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.73811574T>C , CM000679.2:g.73811574T>C	GRCh38
NC_000017.10:g.71807713T>C , CM000679.1:g.71807713T>C	GRCh37
NC_000017.9:g.69319308T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_027146.1:n.228+12114A>G