Canonical Allele Identifier: CA372253651

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145882C>G (hg19) ; chr8:g.133133638C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133638C>G , CM000670.2:g.133133638C>G	GRCh38
NC_000008.10:g.134145882C>G , CM000670.1:g.134145882C>G	GRCh37
NC_000008.9:g.134215064C>G	NCBI36
NG_015832.1:g.271678C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8166C>G MANE Select	ENSP00000220616.4:p.Ile2722Met
ENST00000220616.8:c.8166C>G	ENSP00000220616.4:p.Ile2722Met
ENST00000519178.5:c.3532C>G
ENST00000519543.5:c.2565C>G	ENSP00000430430.1:p.Ile855Met
ENST00000521107.1:c.378C>G	ENSP00000430161.1:p.Ile126Met
ENST00000522691.1:n.252C>G
ENST00000523756.5:c.4821C>G
NM_003235.4:c.8166C>G	NP_003226.4:p.Ile2722Met
XM_005251038.3:c.7974C>G	XP_005251095.1:p.Ile2658Met
XM_006716622.2:c.8103C>G	XP_006716685.1:p.Ile2701Met
XM_005251038.4:c.7974C>G	XP_005251095.1:p.Ile2658Met
XM_006716622.3:c.8103C>G	XP_006716685.1:p.Ile2701Met
XM_017013793.1:c.8100C>G	XP_016869282.1:p.Ile2700Met
XM_017013794.1:c.8031C>G	XP_016869283.1:p.Ile2677Met
XM_017013795.1:c.7995C>G	XP_016869284.1:p.Ile2665Met
XM_017013796.1:c.7947C>G	XP_016869285.1:p.Ile2649Met
XM_017013797.1:c.7905C>G	XP_016869286.1:p.Ile2635Met
NM_003235.5:c.8166C>G MANE Select	NP_003226.4:p.Ile2722Met