Canonical Allele Identifier: CA762147063

Gene: LINC01090

Linked Data

• dbSNP Id: rs7582658
• MyVariant Identifiers: chr2:g.188947841A>C (hg19) ; chr2:g.188083114A>C (hg38)

Genomic Alleles

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

Transcript Alleles

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