Canonical Allele Identifier: CA880387422

Gene: TBL1Y

Linked Data

• dbSNP Id: rs1307918590
• MyVariant Identifiers: chrY:g.6876455A>G (hg19) ; chrY:g.7008414A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.7008414A>G , CM000686.2:g.7008414A>G	GRCh38
NC_000024.9:g.6876455A>G , CM000686.1:g.6876455A>G	GRCh37
NC_000024.8:g.6936455A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000383032.6:c.-140+12516A>G MANE Select	ENSP00000372499.1:n.-140+12516A>G
ENST00000346432.3:c.-139-13035A>G	ENSP00000328879.4:n.-139-13035A>G
ENST00000355162.6:c.-140+12516A>G	ENSP00000347289.2:n.-140+12516A>G
ENST00000383032.5:c.-140+12516A>G	ENSP00000372499.1:n.-140+12516A>G
NM_033284.1:c.-140+12516A>G	NP_150600.1:n.-140+12516A>G
NM_134258.1:c.-140+12516A>G	NP_599020.1:n.-140+12516A>G
NM_134259.1:c.-139-13035A>G	NP_599021.1:n.-139-13035A>G
XM_017030086.1:c.-140+12516A>G	XP_016885575.1:n.-140+12516A>G
XM_017030087.1:c.-140+12516A>G	XP_016885576.1:n.-140+12516A>G
XM_024452497.1:c.-140+12516A>G	XP_024308265.1:n.-140+12516A>G
NM_033284.2:c.-140+12516A>G MANE Select	NP_150600.1:n.-140+12516A>G
NM_134258.2:c.-140+12516A>G	NP_599020.1:n.-140+12516A>G
NM_134259.2:c.-139-13035A>G	NP_599021.1:n.-139-13035A>G