Canonical Allele Identifier: CA372253720

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145904G>T (hg19) ; chr8:g.133133660G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133660G>T , CM000670.2:g.133133660G>T	GRCh38
NC_000008.10:g.134145904G>T , CM000670.1:g.134145904G>T	GRCh37
NC_000008.9:g.134215086G>T	NCBI36
NG_015832.1:g.271700G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8188G>T MANE Select	ENSP00000220616.4:p.Asp2730Tyr
ENST00000220616.8:c.8188G>T	ENSP00000220616.4:p.Asp2730Tyr
ENST00000519178.5:c.3554G>T
ENST00000519543.5:c.2587G>T	ENSP00000430430.1:p.Asp863Tyr
ENST00000521107.1:c.400G>T	ENSP00000430161.1:p.Asp134Tyr
ENST00000522691.1:n.274G>T
ENST00000523756.5:c.4843G>T
NM_003235.4:c.8188G>T	NP_003226.4:p.Asp2730Tyr
XM_005251038.3:c.7996G>T	XP_005251095.1:p.Asp2666Tyr
XM_006716622.2:c.8125G>T	XP_006716685.1:p.Asp2709Tyr
XM_005251038.4:c.7996G>T	XP_005251095.1:p.Asp2666Tyr
XM_006716622.3:c.8125G>T	XP_006716685.1:p.Asp2709Tyr
XM_017013793.1:c.8122G>T	XP_016869282.1:p.Asp2708Tyr
XM_017013794.1:c.8053G>T	XP_016869283.1:p.Asp2685Tyr
XM_017013795.1:c.8017G>T	XP_016869284.1:p.Asp2673Tyr
XM_017013796.1:c.7969G>T	XP_016869285.1:p.Asp2657Tyr
XM_017013797.1:c.7927G>T	XP_016869286.1:p.Asp2643Tyr
NM_003235.5:c.8188G>T MANE Select	NP_003226.4:p.Asp2730Tyr