Canonical Allele Identifier: CA774555011
Gene: LINC01483 HGNC NCBI

Linked Data

dbSNP Id: rs1430019042

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854705A>G , CM000679.2:g.69854705A>G GRCh38
NC_000017.10:g.67850846A>G , CM000679.1:g.67850846A>G GRCh37
NC_000017.9:g.65362441A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109971.1:n.363+9219A>G
NR_109972.1:n.363+9219A>G