Canonical Allele Identifier: CA463017274

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145882C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133638C>A , CM000670.2:g.133133638C>A	GRCh38
NC_000008.10:g.134145882C>A , CM000670.1:g.134145882C>A	GRCh37
NC_000008.9:g.134215064C>A	NCBI36
NG_015832.1:g.271678C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8166C>A MANE Select	ENSP00000220616.4:p.Ile2722=
ENST00000220616.8:c.8166C>A	ENSP00000220616.4:p.Ile2722=
ENST00000519178.5:c.3532C>A
ENST00000519543.5:c.2565C>A	ENSP00000430430.1:p.Ile855=
ENST00000521107.1:c.378C>A	ENSP00000430161.1:p.Ile126=
ENST00000522691.1:n.252C>A
ENST00000523756.5:c.4821C>A
NM_003235.4:c.8166C>A	NP_003226.4:p.Ile2722=
XM_005251038.3:c.7974C>A	XP_005251095.1:p.Ile2658=
XM_006716622.2:c.8103C>A	XP_006716685.1:p.Ile2701=
XM_005251038.4:c.7974C>A	XP_005251095.1:p.Ile2658=
XM_006716622.3:c.8103C>A	XP_006716685.1:p.Ile2701=
XM_017013793.1:c.8100C>A	XP_016869282.1:p.Ile2700=
XM_017013794.1:c.8031C>A	XP_016869283.1:p.Ile2677=
XM_017013795.1:c.7995C>A	XP_016869284.1:p.Ile2665=
XM_017013796.1:c.7947C>A	XP_016869285.1:p.Ile2649=
XM_017013797.1:c.7905C>A	XP_016869286.1:p.Ile2635=
NM_003235.5:c.8166C>A MANE Select	NP_003226.4:p.Ile2722=