Canonical Allele Identifier: CA1357784772
Gene: LINC02033 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.36821489C>G , CM000665.2:g.36821489C>G GRCh38
NC_000003.11:g.36862980C>G , CM000665.1:g.36862980C>G GRCh37
NC_000003.10:g.36837984C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940723.1:n.498-72G>C
NR_147141.1:n.106-72G>C