Canonical Allele Identifier: CA15402046
Gene: LINC01933 HGNC NCBI

Linked Data

dbSNP Id: rs170020

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151964997G>A , CM000667.2:g.151964997G>A GRCh38
NC_000005.9:g.151344558G>A , CM000667.1:g.151344558G>A GRCh37
NC_000005.8:g.151324751G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109876.1:n.57+6043G>A