Canonical Allele Identifier: CA739144148

Gene: UTS2

Linked Data

• dbSNP Id: rs1264396099
• MyVariant Identifiers: chr1:g.7961390G>T (hg19) ; chr1:g.7901330G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7901330G>T , CM000663.2:g.7901330G>T	GRCh38
NC_000001.10:g.7961390G>T , CM000663.1:g.7961390G>T	GRCh37
NC_000001.9:g.7883977G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011540537.1:c.-75+11851C>A	XP_011538839.1:n.-75+11851C>A
XM_011540537.2:c.-75+11851C>A	XP_011538839.1:n.-75+11851C>A
XM_017000116.1:c.-75+11851C>A	XP_016855605.1:n.-75+11851C>A
XM_017000119.1:c.-75+11851C>A	XP_016855608.1:n.-75+11851C>A