Canonical Allele Identifier: CA998319732
Gene: UTS2 HGNC NCBI

Linked Data

dbSNP Id: rs227163
gnomAD v3: 1-7901146-C-A
gnomAD v4: 1-7901146-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7901146C>A , CM000663.2:g.7901146C>A GRCh38
NC_000001.10:g.7961206C>A , CM000663.1:g.7961206C>A GRCh37
NC_000001.9:g.7883793C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011540537.1:c.-75+12035G>T XP_011538839.1:n.-75+12035G>T
XM_011540537.2:c.-75+12035G>T XP_011538839.1:n.-75+12035G>T
XM_017000116.1:c.-75+12035G>T XP_016855605.1:n.-75+12035G>T
XM_017000119.1:c.-75+12035G>T XP_016855608.1:n.-75+12035G>T
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