Canonical Allele Identifier: CA337556068

Gene: TBL1Y

Linked Data

• dbSNP Id: rs968391312
• gnomAD v3: Y-7019232-T-A
• gnomAD v4: Y-7019232-T-A
• MyVariant Identifiers: chrY:g.6887273T>A (hg19) ; chrY:g.7019232T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.7019232T>A , CM000686.2:g.7019232T>A	GRCh38
NC_000024.9:g.6887273T>A , CM000686.1:g.6887273T>A	GRCh37
NC_000024.8:g.6947273T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383032.6:c.-139-2217T>A MANE Select	ENSP00000372499.1:n.-139-2217T>A
ENST00000346432.3:c.-139-2217T>A	ENSP00000328879.4:n.-139-2217T>A
ENST00000355162.6:c.-139-2217T>A	ENSP00000347289.2:n.-139-2217T>A
ENST00000383032.5:c.-139-2217T>A	ENSP00000372499.1:n.-139-2217T>A
NM_033284.1:c.-139-2217T>A	NP_150600.1:n.-139-2217T>A
NM_134258.1:c.-139-2217T>A	NP_599020.1:n.-139-2217T>A
NM_134259.1:c.-139-2217T>A	NP_599021.1:n.-139-2217T>A
XM_017030086.1:c.-139-2217T>A	XP_016885575.1:n.-139-2217T>A
XM_017030087.1:c.-139-2217T>A	XP_016885576.1:n.-139-2217T>A
XM_024452497.1:c.-139-2217T>A	XP_024308265.1:n.-139-2217T>A
NM_033284.2:c.-139-2217T>A MANE Select	NP_150600.1:n.-139-2217T>A
NM_134258.2:c.-139-2217T>A	NP_599020.1:n.-139-2217T>A
NM_134259.2:c.-139-2217T>A	NP_599021.1:n.-139-2217T>A