Canonical Allele Identifier: CA463017073

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145768C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133524C>T , CM000670.2:g.133133524C>T	GRCh38
NC_000008.10:g.134145768C>T , CM000670.1:g.134145768C>T	GRCh37
NC_000008.9:g.134214950C>T	NCBI36
NG_015832.1:g.271564C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8052C>T MANE Select	ENSP00000220616.4:p.Pro2684=
ENST00000220616.8:c.8052C>T	ENSP00000220616.4:p.Pro2684=
ENST00000519178.5:c.3418C>T
ENST00000519543.5:c.2451C>T	ENSP00000430430.1:p.Pro817=
ENST00000521107.1:c.264C>T	ENSP00000430161.1:p.Pro88=
ENST00000522691.1:n.138C>T
ENST00000523756.5:c.4707C>T
NM_003235.4:c.8052C>T	NP_003226.4:p.Pro2684=
XM_005251038.3:c.7860C>T	XP_005251095.1:p.Pro2620=
XM_006716622.2:c.7989C>T	XP_006716685.1:p.Pro2663=
XM_005251038.4:c.7860C>T	XP_005251095.1:p.Pro2620=
XM_006716622.3:c.7989C>T	XP_006716685.1:p.Pro2663=
XM_017013793.1:c.7986C>T	XP_016869282.1:p.Pro2662=
XM_017013794.1:c.7917C>T	XP_016869283.1:p.Pro2639=
XM_017013795.1:c.7881C>T	XP_016869284.1:p.Pro2627=
XM_017013796.1:c.7833C>T	XP_016869285.1:p.Pro2611=
XM_017013797.1:c.7791C>T	XP_016869286.1:p.Pro2597=
NM_003235.5:c.8052C>T MANE Select	NP_003226.4:p.Pro2684=