Canonical Allele Identifier: CA372253629

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145877T>G (hg19) ; chr8:g.133133633T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133633T>G , CM000670.2:g.133133633T>G	GRCh38
NC_000008.10:g.134145877T>G , CM000670.1:g.134145877T>G	GRCh37
NC_000008.9:g.134215059T>G	NCBI36
NG_015832.1:g.271673T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8161T>G MANE Select	ENSP00000220616.4:p.Tyr2721Asp
ENST00000220616.8:c.8161T>G	ENSP00000220616.4:p.Tyr2721Asp
ENST00000519178.5:c.3527T>G
ENST00000519543.5:c.2560T>G	ENSP00000430430.1:p.Tyr854Asp
ENST00000521107.1:c.373T>G	ENSP00000430161.1:p.Tyr125Asp
ENST00000522691.1:n.247T>G
ENST00000523756.5:c.4816T>G
NM_003235.4:c.8161T>G	NP_003226.4:p.Tyr2721Asp
XM_005251038.3:c.7969T>G	XP_005251095.1:p.Tyr2657Asp
XM_006716622.2:c.8098T>G	XP_006716685.1:p.Tyr2700Asp
XM_005251038.4:c.7969T>G	XP_005251095.1:p.Tyr2657Asp
XM_006716622.3:c.8098T>G	XP_006716685.1:p.Tyr2700Asp
XM_017013793.1:c.8095T>G	XP_016869282.1:p.Tyr2699Asp
XM_017013794.1:c.8026T>G	XP_016869283.1:p.Tyr2676Asp
XM_017013795.1:c.7990T>G	XP_016869284.1:p.Tyr2664Asp
XM_017013796.1:c.7942T>G	XP_016869285.1:p.Tyr2648Asp
XM_017013797.1:c.7900T>G	XP_016869286.1:p.Tyr2634Asp
NM_003235.5:c.8161T>G MANE Select	NP_003226.4:p.Tyr2721Asp