Canonical Allele Identifier: CA762147100

Gene: LINC01090

Linked Data

• dbSNP Id: rs905366330
• MyVariant Identifiers: chr2:g.188947884G>T (hg19) ; chr2:g.188083157G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.188083157G>T , CM000664.2:g.188083157G>T	GRCh38
NC_000002.11:g.188947884G>T , CM000664.1:g.188947884G>T	GRCh37
NC_000002.10:g.188656129G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_126396.1:n.381-47446C>A