Canonical Allele Identifier: CA1311720973
Gene: LINC01934 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.181131318A>T , CM000664.2:g.181131318A>T GRCh38
NC_000002.11:g.181996045A>T , CM000664.1:g.181996045A>T GRCh37
NC_000002.10:g.181704290A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130784.1:n.144+7338A>T