Canonical Allele Identifier: CA372253206

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145775G>T (hg19) ; chr8:g.133133531G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133531G>T , CM000670.2:g.133133531G>T	GRCh38
NC_000008.10:g.134145775G>T , CM000670.1:g.134145775G>T	GRCh37
NC_000008.9:g.134214957G>T	NCBI36
NG_015832.1:g.271571G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8059G>T MANE Select	ENSP00000220616.4:p.Asp2687Tyr
ENST00000220616.8:c.8059G>T	ENSP00000220616.4:p.Asp2687Tyr
ENST00000519178.5:c.3425G>T
ENST00000519543.5:c.2458G>T	ENSP00000430430.1:p.Asp820Tyr
ENST00000521107.1:c.271G>T	ENSP00000430161.1:p.Asp91Tyr
ENST00000522691.1:n.145G>T
ENST00000523756.5:c.4714G>T
NM_003235.4:c.8059G>T	NP_003226.4:p.Asp2687Tyr
XM_005251038.3:c.7867G>T	XP_005251095.1:p.Asp2623Tyr
XM_006716622.2:c.7996G>T	XP_006716685.1:p.Asp2666Tyr
XM_005251038.4:c.7867G>T	XP_005251095.1:p.Asp2623Tyr
XM_006716622.3:c.7996G>T	XP_006716685.1:p.Asp2666Tyr
XM_017013793.1:c.7993G>T	XP_016869282.1:p.Asp2665Tyr
XM_017013794.1:c.7924G>T	XP_016869283.1:p.Asp2642Tyr
XM_017013795.1:c.7888G>T	XP_016869284.1:p.Asp2630Tyr
XM_017013796.1:c.7840G>T	XP_016869285.1:p.Asp2614Tyr
XM_017013797.1:c.7798G>T	XP_016869286.1:p.Asp2600Tyr
NM_003235.5:c.8059G>T MANE Select	NP_003226.4:p.Asp2687Tyr