Canonical Allele Identifier: CA11261727

Gene: LINC01090

Linked Data

• dbSNP Id: rs7582658
• gnomAD v2: 2-188947841-A-G
• gnomAD v3: 2-188083114-A-G
• gnomAD v4: 2-188083114-A-G
• MyVariant Identifiers: chr2:g.188947841A>G (hg19) ; chr2:g.188083114A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.188083114A>G , CM000664.2:g.188083114A>G	GRCh38
NC_000002.11:g.188947841A>G , CM000664.1:g.188947841A>G	GRCh37
NC_000002.10:g.188656086A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_126396.1:n.381-47403T>C