Canonical Allele Identifier: CA2272849757
Gene: LINC01483 HGNC NCBI

Linked Data

dbSNP Id: rs1917510070

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854866G>A , CM000679.2:g.69854866G>A GRCh38
NC_000017.10:g.67851007G>A , CM000679.1:g.67851007G>A GRCh37
NC_000017.9:g.65362602G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109971.1:n.363+9380G>A
NR_109972.1:n.363+9380G>A