Canonical Allele Identifier: CA337551989
Gene: TBL1Y HGNC NCBI

Linked Data

dbSNP Id: rs181335666
gnomAD v3: Y-6920150-G-A
gnomAD v4: Y-6920150-G-A
MyVariant Identifiers: chrY:g.6788191G>A (hg19) chrY:g.6920150G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.6920150G>A , CM000686.2:g.6920150G>A GRCh38
NC_000024.9:g.6788191G>A , CM000686.1:g.6788191G>A GRCh37
NC_000024.8:g.6848191G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000383032.6:c.-266+7978G>A MANE Select ENSP00000372499.1:n.-266+7978G>A
ENST00000346432.3:c.-171+7978G>A ENSP00000328879.4:n.-171+7978G>A
ENST00000355162.6:c.-235+7978G>A ENSP00000347289.2:n.-235+7978G>A
ENST00000383032.5:c.-266+7978G>A ENSP00000372499.1:n.-266+7978G>A
NM_033284.1:c.-266+7978G>A NP_150600.1:n.-266+7978G>A
NM_134258.1:c.-235+7978G>A NP_599020.1:n.-235+7978G>A
NM_134259.1:c.-171+7978G>A NP_599021.1:n.-171+7978G>A
XM_017030086.1:c.-266+7978G>A XP_016885575.1:n.-266+7978G>A
XM_017030087.1:c.-266+7978G>A XP_016885576.1:n.-266+7978G>A
XM_024452497.1:c.-266+7978G>A XP_024308265.1:n.-266+7978G>A
NM_033284.2:c.-266+7978G>A MANE Select NP_150600.1:n.-266+7978G>A
NM_134258.2:c.-235+7978G>A NP_599020.1:n.-235+7978G>A
NM_134259.2:c.-171+7978G>A NP_599021.1:n.-171+7978G>A
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