Canonical Allele Identifier: CA1311727813
Gene: LINC01934 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.181143073T= , CM000664.2:g.181143073T= GRCh38
NC_000002.11:g.182007800T= , CM000664.1:g.182007800T= GRCh37
NC_000002.10:g.181716045T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130784.1:n.144+19093T=