Canonical Allele Identifier: CA1152124101
Gene: UTS2 HGNC NCBI

Linked Data

dbSNP Id: rs1639177146

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7901131G>C , CM000663.2:g.7901131G>C GRCh38
NC_000001.10:g.7961191G>C , CM000663.1:g.7961191G>C GRCh37
NC_000001.9:g.7883778G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011540537.1:c.-75+12050C>G XP_011538839.1:n.-75+12050C>G
XM_011540537.2:c.-75+12050C>G XP_011538839.1:n.-75+12050C>G
XM_017000116.1:c.-75+12050C>G XP_016855605.1:n.-75+12050C>G
XM_017000119.1:c.-75+12050C>G XP_016855608.1:n.-75+12050C>G