Canonical Allele Identifier: CA627271675
Gene: LINC01483 HGNC NCBI

Linked Data

dbSNP Id: rs1456459528

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854806del , CM000679.2:g.69854806del GRCh38
NC_000017.10:g.67850947del , CM000679.1:g.67850947del GRCh37
NC_000017.9:g.65362542del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109971.1:n.363+9320del
NR_109972.1:n.363+9320del