Canonical Allele Identifier: CA463017289

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145888T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133644T>G , CM000670.2:g.133133644T>G	GRCh38
NC_000008.10:g.134145888T>G , CM000670.1:g.134145888T>G	GRCh37
NC_000008.9:g.134215070T>G	NCBI36
NG_015832.1:g.271684T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8172T>G MANE Select	ENSP00000220616.4:p.Ser2724=
ENST00000220616.8:c.8172T>G	ENSP00000220616.4:p.Ser2724=
ENST00000519178.5:c.3538T>G
ENST00000519543.5:c.2571T>G	ENSP00000430430.1:p.Ser857=
ENST00000521107.1:c.384T>G	ENSP00000430161.1:p.Ser128=
ENST00000522691.1:n.258T>G
ENST00000523756.5:c.4827T>G
NM_003235.4:c.8172T>G	NP_003226.4:p.Ser2724=
XM_005251038.3:c.7980T>G	XP_005251095.1:p.Ser2660=
XM_006716622.2:c.8109T>G	XP_006716685.1:p.Ser2703=
XM_005251038.4:c.7980T>G	XP_005251095.1:p.Ser2660=
XM_006716622.3:c.8109T>G	XP_006716685.1:p.Ser2703=
XM_017013793.1:c.8106T>G	XP_016869282.1:p.Ser2702=
XM_017013794.1:c.8037T>G	XP_016869283.1:p.Ser2679=
XM_017013795.1:c.8001T>G	XP_016869284.1:p.Ser2667=
XM_017013796.1:c.7953T>G	XP_016869285.1:p.Ser2651=
XM_017013797.1:c.7911T>G	XP_016869286.1:p.Ser2637=
NM_003235.5:c.8172T>G MANE Select	NP_003226.4:p.Ser2724=