Canonical Allele Identifier: CA2272849688
Gene: LINC01483 HGNC NCBI

Linked Data

dbSNP Id: rs1917507076

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854712A>C , CM000679.2:g.69854712A>C GRCh38
NC_000017.10:g.67850853A>C , CM000679.1:g.67850853A>C GRCh37
NC_000017.9:g.65362448A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109971.1:n.363+9226A>C
NR_109972.1:n.363+9226A>C