Canonical Allele Identifier: CA1142447449
Gene: UTS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7901090T= , CM000663.2:g.7901090T= GRCh38
NC_000001.10:g.7961150T= , CM000663.1:g.7961150T= GRCh37
NC_000001.9:g.7883737T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011540537.1:c.-75+12091A= XP_011538839.1:n.-75+12091A=
XM_011540537.2:c.-75+12091A= XP_011538839.1:n.-75+12091A=
XM_017000116.1:c.-75+12091A= XP_016855605.1:n.-75+12091A=
XM_017000119.1:c.-75+12091A= XP_016855608.1:n.-75+12091A=