Canonical Allele Identifier: CA998319741
Gene: UTS2 HGNC NCBI

Linked Data

dbSNP Id: rs1639178597
gnomAD v3: 1-7901204-G-A
gnomAD v4: 1-7901204-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7901204G>A , CM000663.2:g.7901204G>A GRCh38
NC_000001.10:g.7961264G>A , CM000663.1:g.7961264G>A GRCh37
NC_000001.9:g.7883851G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011540537.1:c.-75+11977C>T XP_011538839.1:n.-75+11977C>T
XM_011540537.2:c.-75+11977C>T XP_011538839.1:n.-75+11977C>T
XM_017000116.1:c.-75+11977C>T XP_016855605.1:n.-75+11977C>T
XM_017000119.1:c.-75+11977C>T XP_016855608.1:n.-75+11977C>T
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