Canonical Allele Identifier: CA463017128

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145792T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133548T>G , CM000670.2:g.133133548T>G	GRCh38
NC_000008.10:g.134145792T>G , CM000670.1:g.134145792T>G	GRCh37
NC_000008.9:g.134214974T>G	NCBI36
NG_015832.1:g.271588T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8076T>G MANE Select	ENSP00000220616.4:p.Ala2692=
ENST00000220616.8:c.8076T>G	ENSP00000220616.4:p.Ala2692=
ENST00000519178.5:c.3442T>G
ENST00000519543.5:c.2475T>G	ENSP00000430430.1:p.Ala825=
ENST00000521107.1:c.288T>G	ENSP00000430161.1:p.Ala96=
ENST00000522691.1:n.162T>G
ENST00000523756.5:c.4731T>G
NM_003235.4:c.8076T>G	NP_003226.4:p.Ala2692=
XM_005251038.3:c.7884T>G	XP_005251095.1:p.Ala2628=
XM_006716622.2:c.8013T>G	XP_006716685.1:p.Ala2671=
XM_005251038.4:c.7884T>G	XP_005251095.1:p.Ala2628=
XM_006716622.3:c.8013T>G	XP_006716685.1:p.Ala2671=
XM_017013793.1:c.8010T>G	XP_016869282.1:p.Ala2670=
XM_017013794.1:c.7941T>G	XP_016869283.1:p.Ala2647=
XM_017013795.1:c.7905T>G	XP_016869284.1:p.Ala2635=
XM_017013796.1:c.7857T>G	XP_016869285.1:p.Ala2619=
XM_017013797.1:c.7815T>G	XP_016869286.1:p.Ala2605=
NM_003235.5:c.8076T>G MANE Select	NP_003226.4:p.Ala2692=