Canonical Allele Identifier: CA2272849778
Gene: LINC01483 HGNC NCBI

Linked Data

dbSNP Id: rs1917510705

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854917del , CM000679.2:g.69854917del GRCh38
NC_000017.10:g.67851058del , CM000679.1:g.67851058del GRCh37
NC_000017.9:g.65362653del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109971.1:n.363+9431del
NR_109972.1:n.363+9431del