Canonical Allele Identifier: CA463017320

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145903A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133659A>T , CM000670.2:g.133133659A>T	GRCh38
NC_000008.10:g.134145903A>T , CM000670.1:g.134145903A>T	GRCh37
NC_000008.9:g.134215085A>T	NCBI36
NG_015832.1:g.271699A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8187A>T MANE Select	ENSP00000220616.4:p.Ala2729=
ENST00000220616.8:c.8187A>T	ENSP00000220616.4:p.Ala2729=
ENST00000519178.5:c.3553A>T
ENST00000519543.5:c.2586A>T	ENSP00000430430.1:p.Ala862=
ENST00000521107.1:c.399A>T	ENSP00000430161.1:p.Ala133=
ENST00000522691.1:n.273A>T
ENST00000523756.5:c.4842A>T
NM_003235.4:c.8187A>T	NP_003226.4:p.Ala2729=
XM_005251038.3:c.7995A>T	XP_005251095.1:p.Ala2665=
XM_006716622.2:c.8124A>T	XP_006716685.1:p.Ala2708=
XM_005251038.4:c.7995A>T	XP_005251095.1:p.Ala2665=
XM_006716622.3:c.8124A>T	XP_006716685.1:p.Ala2708=
XM_017013793.1:c.8121A>T	XP_016869282.1:p.Ala2707=
XM_017013794.1:c.8052A>T	XP_016869283.1:p.Ala2684=
XM_017013795.1:c.8016A>T	XP_016869284.1:p.Ala2672=
XM_017013796.1:c.7968A>T	XP_016869285.1:p.Ala2656=
XM_017013797.1:c.7926A>T	XP_016869286.1:p.Ala2642=
NM_003235.5:c.8187A>T MANE Select	NP_003226.4:p.Ala2729=