Canonical Allele Identifier: CA463017051

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145756A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133512A>T , CM000670.2:g.133133512A>T	GRCh38
NC_000008.10:g.134145756A>T , CM000670.1:g.134145756A>T	GRCh37
NC_000008.9:g.134214938A>T	NCBI36
NG_015832.1:g.271552A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8040A>T MANE Select	ENSP00000220616.4:p.Thr2680=
ENST00000220616.8:c.8040A>T	ENSP00000220616.4:p.Thr2680=
ENST00000519178.5:c.3406A>T
ENST00000519543.5:c.2439A>T	ENSP00000430430.1:p.Thr813=
ENST00000521107.1:c.252A>T	ENSP00000430161.1:p.Thr84=
ENST00000522691.1:n.126A>T
ENST00000523756.5:c.4695A>T
NM_003235.4:c.8040A>T	NP_003226.4:p.Thr2680=
XM_005251038.3:c.7848A>T	XP_005251095.1:p.Thr2616=
XM_006716622.2:c.7977A>T	XP_006716685.1:p.Thr2659=
XM_005251038.4:c.7848A>T	XP_005251095.1:p.Thr2616=
XM_006716622.3:c.7977A>T	XP_006716685.1:p.Thr2659=
XM_017013793.1:c.7974A>T	XP_016869282.1:p.Thr2658=
XM_017013794.1:c.7905A>T	XP_016869283.1:p.Thr2635=
XM_017013795.1:c.7869A>T	XP_016869284.1:p.Thr2623=
XM_017013796.1:c.7821A>T	XP_016869285.1:p.Thr2607=
XM_017013797.1:c.7779A>T	XP_016869286.1:p.Thr2593=
NM_003235.5:c.8040A>T MANE Select	NP_003226.4:p.Thr2680=