Canonical Allele Identifier: CA337573832
Gene: TBL1Y HGNC NCBI

Linked Data

dbSNP Id: rs113325051
gnomAD v3: Y-7087827-A-C
gnomAD v4: Y-7087827-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7087827A>C , CM000686.2:g.7087827A>C GRCh38
NC_000024.9:g.6955868A>C , CM000686.1:g.6955868A>C GRCh37
NC_000024.8:g.7015868A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000383032.6:c.1446+395A>C MANE Select ENSP00000372499.1:n.1446+395A>C
ENST00000651523.1:c.203+395A>C
ENST00000346432.3:c.1446+395A>C ENSP00000328879.4:n.1446+395A>C
ENST00000355162.6:c.1446+395A>C ENSP00000347289.2:n.1446+395A>C
ENST00000383032.5:c.1446+395A>C ENSP00000372499.1:n.1446+395A>C
NM_033284.1:c.1446+395A>C NP_150600.1:n.1446+395A>C
NM_134258.1:c.1446+395A>C NP_599020.1:n.1446+395A>C
NM_134259.1:c.1446+395A>C NP_599021.1:n.1446+395A>C
XM_005262572.2:c.1488+395A>C XP_005262629.1:n.1488+395A>C
XM_005262572.3:c.1488+395A>C XP_005262629.1:n.1488+395A>C
XM_017030086.1:c.1446+395A>C XP_016885575.1:n.1446+395A>C
XM_017030087.1:c.1446+395A>C XP_016885576.1:n.1446+395A>C
XM_024452497.1:c.1446+395A>C XP_024308265.1:n.1446+395A>C
NM_033284.2:c.1446+395A>C MANE Select NP_150600.1:n.1446+395A>C
NM_134258.2:c.1446+395A>C NP_599020.1:n.1446+395A>C
NM_134259.2:c.1446+395A>C NP_599021.1:n.1446+395A>C