Canonical Allele Identifier: CA372238177

Gene: TG

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133029907G>C , CM000670.2:g.133029907G>C	GRCh38
NC_000008.10:g.134042152G>C , CM000670.1:g.134042152G>C	GRCh37
NC_000008.9:g.134111334G>C	NCBI36
NG_015832.1:g.167948G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.7123G>C MANE Select	ENSP00000220616.4:p.Gly2375Arg
ENST00000220616.8:c.7123G>C	ENSP00000220616.4:p.Gly2375Arg
ENST00000518108.1:c.509G>C
ENST00000519178.5:c.2489G>C
ENST00000519543.5:c.1522G>C	ENSP00000430430.1:p.Gly508Arg
ENST00000523756.5:c.3778G>C
NM_003235.4:c.7123G>C	NP_003226.4:p.Gly2375Arg
XM_005251038.3:c.6931G>C	XP_005251095.1:p.Gly2311Arg
XM_006716622.2:c.7060G>C	XP_006716685.1:p.Gly2354Arg
XM_005251038.4:c.6931G>C	XP_005251095.1:p.Gly2311Arg
XM_006716622.3:c.7060G>C	XP_006716685.1:p.Gly2354Arg
XM_017013793.1:c.7057G>C	XP_016869282.1:p.Gly2353Arg
XM_017013794.1:c.7123G>C	XP_016869283.1:p.Gly2375Arg
XM_017013795.1:c.6952G>C	XP_016869284.1:p.Gly2318Arg
XM_017013796.1:c.6904G>C	XP_016869285.1:p.Gly2302Arg
XM_017013797.1:c.6862G>C	XP_016869286.1:p.Gly2288Arg
XM_017013798.1:c.7123G>C	XP_016869287.1:p.Gly2375Arg
NM_003235.5:c.7123G>C MANE Select	NP_003226.4:p.Gly2375Arg