Canonical Allele Identifier: CA372253077

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145740C>G (hg19) ; chr8:g.133133496C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133496C>G , CM000670.2:g.133133496C>G	GRCh38
NC_000008.10:g.134145740C>G , CM000670.1:g.134145740C>G	GRCh37
NC_000008.9:g.134214922C>G	NCBI36
NG_015832.1:g.271536C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8024C>G MANE Select	ENSP00000220616.4:p.Ser2675Ter
ENST00000220616.8:c.8024C>G	ENSP00000220616.4:p.Ser2675Ter
ENST00000519178.5:c.3390C>G
ENST00000519543.5:c.2423C>G	ENSP00000430430.1:p.Ser808Ter
ENST00000521107.1:c.236C>G	ENSP00000430161.1:p.Ser79Ter
ENST00000522691.1:n.110C>G
ENST00000523756.5:c.4679C>G
NM_003235.4:c.8024C>G	NP_003226.4:p.Ser2675Ter
XM_005251038.3:c.7832C>G	XP_005251095.1:p.Ser2611Ter
XM_006716622.2:c.7961C>G	XP_006716685.1:p.Ser2654Ter
XM_005251038.4:c.7832C>G	XP_005251095.1:p.Ser2611Ter
XM_006716622.3:c.7961C>G	XP_006716685.1:p.Ser2654Ter
XM_017013793.1:c.7958C>G	XP_016869282.1:p.Ser2653Ter
XM_017013794.1:c.7889C>G	XP_016869283.1:p.Ser2630Ter
XM_017013795.1:c.7853C>G	XP_016869284.1:p.Ser2618Ter
XM_017013796.1:c.7805C>G	XP_016869285.1:p.Ser2602Ter
XM_017013797.1:c.7763C>G	XP_016869286.1:p.Ser2588Ter
NM_003235.5:c.8024C>G MANE Select	NP_003226.4:p.Ser2675Ter