Canonical Allele Identifier: CA372233786

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134030196C>A (hg19) ; chr8:g.133017951C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133017951C>A , CM000670.2:g.133017951C>A	GRCh38
NC_000008.10:g.134030196C>A , CM000670.1:g.134030196C>A	GRCh37
NC_000008.9:g.134099378C>A	NCBI36
NG_015832.1:g.155992C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6736C>A MANE Select	ENSP00000220616.4:p.Pro2246Thr
ENST00000220616.8:c.6736C>A	ENSP00000220616.4:p.Pro2246Thr
ENST00000518108.1:c.168+85C>A
ENST00000519178.5:c.2102C>A
ENST00000519543.5:c.1135C>A	ENSP00000430430.1:p.Pro379Thr
ENST00000522523.5:n.797C>A
ENST00000523756.5:c.3391C>A
NM_003235.4:c.6736C>A	NP_003226.4:p.Pro2246Thr
XM_005251038.3:c.6544C>A	XP_005251095.1:p.Pro2182Thr
XM_006716622.2:c.6673C>A	XP_006716685.1:p.Pro2225Thr
XM_005251038.4:c.6544C>A	XP_005251095.1:p.Pro2182Thr
XM_006716622.3:c.6673C>A	XP_006716685.1:p.Pro2225Thr
XM_017013793.1:c.6670C>A	XP_016869282.1:p.Pro2224Thr
XM_017013794.1:c.6736C>A	XP_016869283.1:p.Pro2246Thr
XM_017013795.1:c.6565C>A	XP_016869284.1:p.Pro2189Thr
XM_017013796.1:c.6517C>A	XP_016869285.1:p.Pro2173Thr
XM_017013797.1:c.6475C>A	XP_016869286.1:p.Pro2159Thr
XM_017013798.1:c.6736C>A	XP_016869287.1:p.Pro2246Thr
NM_003235.5:c.6736C>A MANE Select	NP_003226.4:p.Pro2246Thr