Canonical Allele Identifier: CA2272849693
Gene: LINC01483 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854721C= , CM000679.2:g.69854721C= GRCh38
NC_000017.10:g.67850862C= , CM000679.1:g.67850862C= GRCh37
NC_000017.9:g.65362457C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109971.1:n.363+9235C=
NR_109972.1:n.363+9235C=