Canonical Allele Identifier: CA17270697

Gene: UTS2

Linked Data

• dbSNP Id: rs57597442
• gnomAD v2: 1-7961229-A-G
• gnomAD v3: 1-7901169-A-G
• gnomAD v4: 1-7901169-A-G
• MyVariant Identifiers: chr1:g.7961229A>G (hg19) ; chr1:g.7901169A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7901169A>G , CM000663.2:g.7901169A>G	GRCh38
NC_000001.10:g.7961229A>G , CM000663.1:g.7961229A>G	GRCh37
NC_000001.9:g.7883816A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011540537.1:c.-75+12012T>C	XP_011538839.1:n.-75+12012T>C
XM_011540537.2:c.-75+12012T>C	XP_011538839.1:n.-75+12012T>C
XM_017000116.1:c.-75+12012T>C	XP_016855605.1:n.-75+12012T>C
XM_017000119.1:c.-75+12012T>C	XP_016855608.1:n.-75+12012T>C