Canonical Allele Identifier: CA372253597

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145871T>A (hg19) ; chr8:g.133133627T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133627T>A , CM000670.2:g.133133627T>A	GRCh38
NC_000008.10:g.134145871T>A , CM000670.1:g.134145871T>A	GRCh37
NC_000008.9:g.134215053T>A	NCBI36
NG_015832.1:g.271667T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8155T>A MANE Select	ENSP00000220616.4:p.Ser2719Thr
ENST00000220616.8:c.8155T>A	ENSP00000220616.4:p.Ser2719Thr
ENST00000519178.5:c.3521T>A
ENST00000519543.5:c.2554T>A	ENSP00000430430.1:p.Ser852Thr
ENST00000521107.1:c.367T>A	ENSP00000430161.1:p.Ser123Thr
ENST00000522691.1:n.241T>A
ENST00000523756.5:c.4810T>A
NM_003235.4:c.8155T>A	NP_003226.4:p.Ser2719Thr
XM_005251038.3:c.7963T>A	XP_005251095.1:p.Ser2655Thr
XM_006716622.2:c.8092T>A	XP_006716685.1:p.Ser2698Thr
XM_005251038.4:c.7963T>A	XP_005251095.1:p.Ser2655Thr
XM_006716622.3:c.8092T>A	XP_006716685.1:p.Ser2698Thr
XM_017013793.1:c.8089T>A	XP_016869282.1:p.Ser2697Thr
XM_017013794.1:c.8020T>A	XP_016869283.1:p.Ser2674Thr
XM_017013795.1:c.7984T>A	XP_016869284.1:p.Ser2662Thr
XM_017013796.1:c.7936T>A	XP_016869285.1:p.Ser2646Thr
XM_017013797.1:c.7894T>A	XP_016869286.1:p.Ser2632Thr
NM_003235.5:c.8155T>A MANE Select	NP_003226.4:p.Ser2719Thr