Canonical Allele Identifier: CA520783898
Gene: UTS2 HGNC NCBI

Linked Data

dbSNP Id: rs1183910245
gnomAD v2: 1-7961414-GGGT-G
gnomAD v3: 1-7901354-GGGT-G
gnomAD v4: 1-7901354-GGGT-G
MyVariant Identifiers: chr1:g.7961415_7961417del (hg19) chr1:g.7901355_7901357del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7901359_7901361del , CM000663.2:g.7901359_7901361del GRCh38
NC_000001.10:g.7961419_7961421del , CM000663.1:g.7961419_7961421del GRCh37
NC_000001.9:g.7884006_7884008del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011540537.1:c.-75+11824_-75+11826del XP_011538839.1:n.-75+11824_-75+11826del
XM_011540537.2:c.-75+11824_-75+11826del XP_011538839.1:n.-75+11824_-75+11826del
XM_017000116.1:c.-75+11824_-75+11826del XP_016855605.1:n.-75+11824_-75+11826del
XM_017000119.1:c.-75+11824_-75+11826del XP_016855608.1:n.-75+11824_-75+11826del
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