Canonical Allele Identifier: CA1152124417
Gene: UTS2 HGNC NCBI

Linked Data

dbSNP Id: rs1639181295

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7901298G>A , CM000663.2:g.7901298G>A GRCh38
NC_000001.10:g.7961358G>A , CM000663.1:g.7961358G>A GRCh37
NC_000001.9:g.7883945G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011540537.1:c.-75+11883C>T XP_011538839.1:n.-75+11883C>T
XM_011540537.2:c.-75+11883C>T XP_011538839.1:n.-75+11883C>T
XM_017000116.1:c.-75+11883C>T XP_016855605.1:n.-75+11883C>T
XM_017000119.1:c.-75+11883C>T XP_016855608.1:n.-75+11883C>T