Canonical Allele Identifier: CA739144075
Gene: UTS2 HGNC NCBI

Linked Data

dbSNP Id: rs1016333797
gnomAD v3: 1-7901135-T-G
gnomAD v4: 1-7901135-T-G
MyVariant Identifiers: chr1:g.7961195T>G (hg19) chr1:g.7901135T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7901135T>G , CM000663.2:g.7901135T>G GRCh38
NC_000001.10:g.7961195T>G , CM000663.1:g.7961195T>G GRCh37
NC_000001.9:g.7883782T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011540537.1:c.-75+12046A>C XP_011538839.1:n.-75+12046A>C
XM_011540537.2:c.-75+12046A>C XP_011538839.1:n.-75+12046A>C
XM_017000116.1:c.-75+12046A>C XP_016855605.1:n.-75+12046A>C
XM_017000119.1:c.-75+12046A>C XP_016855608.1:n.-75+12046A>C
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