Canonical Allele Identifier: CA4885890

Gene: TG

Linked Data

• dbSNP Id: rs750756628
• ExAC: 8:134145800 A / T
• gnomAD v2: 8-134145800-A-T
• MyVariant Identifiers: chr8:g.134145800A>T (hg19) ; chr8:g.133133556A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133556A>T , CM000670.2:g.133133556A>T	GRCh38
NC_000008.10:g.134145800A>T , CM000670.1:g.134145800A>T	GRCh37
NC_000008.9:g.134214982A>T	NCBI36
NG_015832.1:g.271596A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8084A>T MANE Select	ENSP00000220616.4:p.Glu2695Val
ENST00000220616.8:c.8084A>T	ENSP00000220616.4:p.Glu2695Val
ENST00000519178.5:c.3450A>T
ENST00000519543.5:c.2483A>T	ENSP00000430430.1:p.Glu828Val
ENST00000521107.1:c.296A>T	ENSP00000430161.1:p.Glu99Val
ENST00000522691.1:n.170A>T
ENST00000523756.5:c.4739A>T
NM_003235.4:c.8084A>T	NP_003226.4:p.Glu2695Val
XM_005251038.3:c.7892A>T	XP_005251095.1:p.Glu2631Val
XM_006716622.2:c.8021A>T	XP_006716685.1:p.Glu2674Val
XM_005251038.4:c.7892A>T	XP_005251095.1:p.Glu2631Val
XM_006716622.3:c.8021A>T	XP_006716685.1:p.Glu2674Val
XM_017013793.1:c.8018A>T	XP_016869282.1:p.Glu2673Val
XM_017013794.1:c.7949A>T	XP_016869283.1:p.Glu2650Val
XM_017013795.1:c.7913A>T	XP_016869284.1:p.Glu2638Val
XM_017013796.1:c.7865A>T	XP_016869285.1:p.Glu2622Val
XM_017013797.1:c.7823A>T	XP_016869286.1:p.Glu2608Val
NM_003235.5:c.8084A>T MANE Select	NP_003226.4:p.Glu2695Val