Canonical Allele Identifier: CA1152124178
Gene: UTS2 HGNC NCBI

Linked Data

dbSNP Id: rs1639177925
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7901163dup , CM000663.2:g.7901163dup GRCh38
NC_000001.10:g.7961223dup , CM000663.1:g.7961223dup GRCh37
NC_000001.9:g.7883810dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011540537.1:c.-75+12019dup XP_011538839.1:n.-75+12019dup
XM_011540537.2:c.-75+12019dup XP_011538839.1:n.-75+12019dup
XM_017000116.1:c.-75+12019dup XP_016855605.1:n.-75+12019dup
XM_017000119.1:c.-75+12019dup XP_016855608.1:n.-75+12019dup
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