Canonical Allele Identifier: CA1152124311
Gene: UTS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7901239T= , CM000663.2:g.7901239T= GRCh38
NC_000001.10:g.7961299T= , CM000663.1:g.7961299T= GRCh37
NC_000001.9:g.7883886T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011540537.1:c.-75+11942A= XP_011538839.1:n.-75+11942A=
XM_011540537.2:c.-75+11942A= XP_011538839.1:n.-75+11942A=
XM_017000116.1:c.-75+11942A= XP_016855605.1:n.-75+11942A=
XM_017000119.1:c.-75+11942A= XP_016855608.1:n.-75+11942A=