Canonical Allele Identifier: CA774933159

Gene: LINC00469

Linked Data

• dbSNP Id: rs754959399
• gnomAD v3: 17-73811559-C-G
• gnomAD v4: 17-73811559-C-G
• MyVariant Identifiers: chr17:g.71807698C>G (hg19) ; chr17:g.73811559C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.73811559C>G , CM000679.2:g.73811559C>G	GRCh38
NC_000017.10:g.71807698C>G , CM000679.1:g.71807698C>G	GRCh37
NC_000017.9:g.69319293C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_027146.1:n.228+12129G>C