Canonical Allele Identifier: CA337727705
Gene: UTY HGNC NCBI

Linked Data

dbSNP Id: rs112028482
gnomAD v3: Y-13233106-C-T
gnomAD v4: Y-13233106-C-T
MyVariant Identifiers: chrY:g.15344987C>T (hg19) chrY:g.13233106C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13233106C>T , CM000686.2:g.13233106C>T GRCh38
NC_000024.9:g.15344987C>T , CM000686.1:g.15344987C>T GRCh37
NC_000024.8:g.13854381C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011531441.3:c.*1280G>A XP_011529743.1:n.*1280G>A
XM_011531442.3:c.*1280G>A XP_011529744.1:n.*1280G>A
XM_011531443.3:c.*1280G>A XP_011529745.1:n.*1280G>A
XM_011531445.3:c.*1280G>A XP_011529747.1:n.*1280G>A
XM_011531446.3:c.*1280G>A XP_011529748.1:n.*1280G>A
XM_011531447.3:c.*1280G>A XP_011529749.1:n.*1280G>A
XM_011531448.3:c.*1280G>A XP_011529750.1:n.*1280G>A
XM_011531449.3:c.*1280G>A XP_011529751.1:n.*1280G>A
XM_011531450.3:c.*1280G>A XP_011529752.1:n.*1280G>A
XM_011531451.3:c.*1280G>A XP_011529753.1:n.*1280G>A
XM_011531452.3:c.*1280G>A XP_011529754.1:n.*1280G>A
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