Canonical Allele Identifier: CA463017196

Gene: TG

Linked Data

• gnomAD v4: 8-133133587-C-T
• MyVariant Identifiers: chr8:g.134145831C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133587C>T , CM000670.2:g.133133587C>T	GRCh38
NC_000008.10:g.134145831C>T , CM000670.1:g.134145831C>T	GRCh37
NC_000008.9:g.134215013C>T	NCBI36
NG_015832.1:g.271627C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8115C>T MANE Select	ENSP00000220616.4:p.Pro2705=
ENST00000220616.8:c.8115C>T	ENSP00000220616.4:p.Pro2705=
ENST00000519178.5:c.3481C>T
ENST00000519543.5:c.2514C>T	ENSP00000430430.1:p.Pro838=
ENST00000521107.1:c.327C>T	ENSP00000430161.1:p.Pro109=
ENST00000522691.1:n.201C>T
ENST00000523756.5:c.4770C>T
NM_003235.4:c.8115C>T	NP_003226.4:p.Pro2705=
XM_005251038.3:c.7923C>T	XP_005251095.1:p.Pro2641=
XM_006716622.2:c.8052C>T	XP_006716685.1:p.Pro2684=
XM_005251038.4:c.7923C>T	XP_005251095.1:p.Pro2641=
XM_006716622.3:c.8052C>T	XP_006716685.1:p.Pro2684=
XM_017013793.1:c.8049C>T	XP_016869282.1:p.Pro2683=
XM_017013794.1:c.7980C>T	XP_016869283.1:p.Pro2660=
XM_017013795.1:c.7944C>T	XP_016869284.1:p.Pro2648=
XM_017013796.1:c.7896C>T	XP_016869285.1:p.Pro2632=
XM_017013797.1:c.7854C>T	XP_016869286.1:p.Pro2618=
NM_003235.5:c.8115C>T MANE Select	NP_003226.4:p.Pro2705=