Canonical Allele Identifier: CA2695508988
Gene: UTS2 HGNC NCBI

Linked Data

dbSNP Id: rs2151400465

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7901294dup , CM000663.2:g.7901294dup GRCh38
NC_000001.10:g.7961354dup , CM000663.1:g.7961354dup GRCh37
NC_000001.9:g.7883941dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011540537.1:c.-75+11887dup XP_011538839.1:n.-75+11887dup
XM_011540537.2:c.-75+11887dup XP_011538839.1:n.-75+11887dup
XM_017000116.1:c.-75+11887dup XP_016855605.1:n.-75+11887dup
XM_017000119.1:c.-75+11887dup XP_016855608.1:n.-75+11887dup