Canonical Allele Identifier: CA739144098

Gene: UTS2

Linked Data

• dbSNP Id: rs1264185988
• gnomAD v3: 1-7901170-T-C
• gnomAD v4: 1-7901170-T-C
• MyVariant Identifiers: chr1:g.7961230T>C (hg19) ; chr1:g.7901170T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7901170T>C , CM000663.2:g.7901170T>C	GRCh38
NC_000001.10:g.7961230T>C , CM000663.1:g.7961230T>C	GRCh37
NC_000001.9:g.7883817T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011540537.1:c.-75+12011A>G	XP_011538839.1:n.-75+12011A>G
XM_011540537.2:c.-75+12011A>G	XP_011538839.1:n.-75+12011A>G
XM_017000116.1:c.-75+12011A>G	XP_016855605.1:n.-75+12011A>G
XM_017000119.1:c.-75+12011A>G	XP_016855608.1:n.-75+12011A>G