Canonical Allele Identifier: CA372253296

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145799G>T (hg19) ; chr8:g.133133555G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133555G>T , CM000670.2:g.133133555G>T	GRCh38
NC_000008.10:g.134145799G>T , CM000670.1:g.134145799G>T	GRCh37
NC_000008.9:g.134214981G>T	NCBI36
NG_015832.1:g.271595G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8083G>T MANE Select	ENSP00000220616.4:p.Glu2695Ter
ENST00000220616.8:c.8083G>T	ENSP00000220616.4:p.Glu2695Ter
ENST00000519178.5:c.3449G>T
ENST00000519543.5:c.2482G>T	ENSP00000430430.1:p.Glu828Ter
ENST00000521107.1:c.295G>T	ENSP00000430161.1:p.Glu99Ter
ENST00000522691.1:n.169G>T
ENST00000523756.5:c.4738G>T
NM_003235.4:c.8083G>T	NP_003226.4:p.Glu2695Ter
XM_005251038.3:c.7891G>T	XP_005251095.1:p.Glu2631Ter
XM_006716622.2:c.8020G>T	XP_006716685.1:p.Glu2674Ter
XM_005251038.4:c.7891G>T	XP_005251095.1:p.Glu2631Ter
XM_006716622.3:c.8020G>T	XP_006716685.1:p.Glu2674Ter
XM_017013793.1:c.8017G>T	XP_016869282.1:p.Glu2673Ter
XM_017013794.1:c.7948G>T	XP_016869283.1:p.Glu2650Ter
XM_017013795.1:c.7912G>T	XP_016869284.1:p.Glu2638Ter
XM_017013796.1:c.7864G>T	XP_016869285.1:p.Glu2622Ter
XM_017013797.1:c.7822G>T	XP_016869286.1:p.Glu2608Ter
NM_003235.5:c.8083G>T MANE Select	NP_003226.4:p.Glu2695Ter