Canonical Allele Identifier: CA2272849678
Gene: LINC01483 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854699G= , CM000679.2:g.69854699G= GRCh38
NC_000017.10:g.67850840G= , CM000679.1:g.67850840G= GRCh37
NC_000017.9:g.65362435G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109971.1:n.363+9213G=
NR_109972.1:n.363+9213G=