Canonical Allele Identifier: CA739144093

Gene: UTS2

Linked Data

• dbSNP Id: rs1301199577
• gnomAD v3: 1-7901167-G-A
• gnomAD v4: 1-7901167-G-A
• MyVariant Identifiers: chr1:g.7961227G>A (hg19) ; chr1:g.7901167G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7901167G>A , CM000663.2:g.7901167G>A	GRCh38
NC_000001.10:g.7961227G>A , CM000663.1:g.7961227G>A	GRCh37
NC_000001.9:g.7883814G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011540537.1:c.-75+12014C>T	XP_011538839.1:n.-75+12014C>T
XM_011540537.2:c.-75+12014C>T	XP_011538839.1:n.-75+12014C>T
XM_017000116.1:c.-75+12014C>T	XP_016855605.1:n.-75+12014C>T
XM_017000119.1:c.-75+12014C>T	XP_016855608.1:n.-75+12014C>T