Canonical Allele Identifier: CA293666648

Gene: LINC01483

Linked Data

• dbSNP Id: rs773397094
• MyVariant Identifiers: chr17:g.67850769A>G (hg19) ; chr17:g.69854628A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.69854628A>G , CM000679.2:g.69854628A>G	GRCh38
NC_000017.10:g.67850769A>G , CM000679.1:g.67850769A>G	GRCh37
NC_000017.9:g.65362364A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109971.1:n.363+9142A>G
NR_109972.1:n.363+9142A>G