Canonical Allele Identifier: CA1152124211
Gene: UTS2 HGNC NCBI

Linked Data

dbSNP Id: rs1639178396

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7901185C>G , CM000663.2:g.7901185C>G GRCh38
NC_000001.10:g.7961245C>G , CM000663.1:g.7961245C>G GRCh37
NC_000001.9:g.7883832C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011540537.1:c.-75+11996G>C XP_011538839.1:n.-75+11996G>C
XM_011540537.2:c.-75+11996G>C XP_011538839.1:n.-75+11996G>C
XM_017000116.1:c.-75+11996G>C XP_016855605.1:n.-75+11996G>C
XM_017000119.1:c.-75+11996G>C XP_016855608.1:n.-75+11996G>C