Canonical Allele Identifier: CA463012093

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.133975288A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132963043A>T , CM000670.2:g.132963043A>T	GRCh38
NC_000008.10:g.133975288A>T , CM000670.1:g.133975288A>T	GRCh37
NC_000008.9:g.134044470A>T	NCBI36
NG_015832.1:g.101084A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000220616.9:c.5517A>T MANE Select	ENSP00000220616.4:p.Thr1839=
ENST00000220616.8:c.5517A>T	ENSP00000220616.4:p.Thr1839=
ENST00000518058.1:c.50A>T
ENST00000519178.5:c.883A>T
ENST00000523756.5:c.2172A>T
NM_003235.4:c.5517A>T	NP_003226.4:p.Thr1839=
XM_005251038.3:c.5325A>T	XP_005251095.1:p.Thr1775=
XM_005251040.3:c.5517A>T	XP_005251097.1:p.Thr1839=
XM_005251042.3:c.5517A>T	XP_005251099.1:p.Thr1839=
XM_005251043.3:c.5517A>T	XP_005251100.1:p.Thr1839=
XM_006716622.2:c.5517A>T	XP_006716685.1:p.Thr1839=
XM_005251038.4:c.5325A>T	XP_005251095.1:p.Thr1775=
XM_005251040.4:c.5517A>T	XP_005251097.1:p.Thr1839=
XM_005251042.4:c.5517A>T	XP_005251099.1:p.Thr1839=
XM_006716622.3:c.5517A>T	XP_006716685.1:p.Thr1839=
XM_017013793.1:c.5451A>T	XP_016869282.1:p.Thr1817=
XM_017013794.1:c.5517A>T	XP_016869283.1:p.Thr1839=
XM_017013795.1:c.5346A>T	XP_016869284.1:p.Thr1782=
XM_017013796.1:c.5298A>T	XP_016869285.1:p.Thr1766=
XM_017013797.1:c.5256A>T	XP_016869286.1:p.Thr1752=
XM_017013798.1:c.5517A>T	XP_016869287.1:p.Thr1839=
XM_017013799.1:c.5517A>T	XP_016869288.1:p.Thr1839=
XM_017013800.1:c.5517A>T	XP_016869289.1:p.Thr1839=
NM_003235.5:c.5517A>T MANE Select	NP_003226.4:p.Thr1839=