Canonical Allele Identifier: CA62003679

Gene: LINC01090

Linked Data

• dbSNP Id: rs912523990
• gnomAD v2: 2-188947851-T-A
• gnomAD v3: 2-188083124-T-A
• gnomAD v4: 2-188083124-T-A
• MyVariant Identifiers: chr2:g.188947851T>A (hg19) ; chr2:g.188083124T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.188083124T>A , CM000664.2:g.188083124T>A	GRCh38
NC_000002.11:g.188947851T>A , CM000664.1:g.188947851T>A	GRCh37
NC_000002.10:g.188656096T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_126396.1:n.381-47413A>T