Canonical Allele Identifier: CA998319713
Gene: UTS2 HGNC NCBI

Linked Data

dbSNP Id: rs1639176599
gnomAD v3: 1-7901089-G-GT
gnomAD v4: 1-7901089-G-GT
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7901095dup , CM000663.2:g.7901095dup GRCh38
NC_000001.10:g.7961155dup , CM000663.1:g.7961155dup GRCh37
NC_000001.9:g.7883742dup NCBI36

Transcript Alleles

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