Canonical Allele Identifier: CA774555000

Gene: LINC01483

Linked Data

• dbSNP Id: rs1274326933
• gnomAD v3: 17-69854654-C-A
• gnomAD v4: 17-69854654-C-A
• MyVariant Identifiers: chr17:g.67850795C>A (hg19) ; chr17:g.69854654C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.69854654C>A , CM000679.2:g.69854654C>A	GRCh38
NC_000017.10:g.67850795C>A , CM000679.1:g.67850795C>A	GRCh37
NC_000017.9:g.65362390C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109971.1:n.363+9168C>A
NR_109972.1:n.363+9168C>A