Canonical Allele Identifier: CA739144082
Gene: UTS2 HGNC NCBI

Linked Data

dbSNP Id: rs972186149
MyVariant Identifiers: chr1:g.7961203A>T (hg19) chr1:g.7901143A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7901143A>T , CM000663.2:g.7901143A>T GRCh38
NC_000001.10:g.7961203A>T , CM000663.1:g.7961203A>T GRCh37
NC_000001.9:g.7883790A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011540537.1:c.-75+12038T>A XP_011538839.1:n.-75+12038T>A
XM_011540537.2:c.-75+12038T>A XP_011538839.1:n.-75+12038T>A
XM_017000116.1:c.-75+12038T>A XP_016855605.1:n.-75+12038T>A
XM_017000119.1:c.-75+12038T>A XP_016855608.1:n.-75+12038T>A
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