Canonical Allele Identifier: CA372253579

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145868T>G (hg19) ; chr8:g.133133624T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133624T>G , CM000670.2:g.133133624T>G	GRCh38
NC_000008.10:g.134145868T>G , CM000670.1:g.134145868T>G	GRCh37
NC_000008.9:g.134215050T>G	NCBI36
NG_015832.1:g.271664T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8152T>G MANE Select	ENSP00000220616.4:p.Trp2718Gly
ENST00000220616.8:c.8152T>G	ENSP00000220616.4:p.Trp2718Gly
ENST00000519178.5:c.3518T>G
ENST00000519543.5:c.2551T>G	ENSP00000430430.1:p.Trp851Gly
ENST00000521107.1:c.364T>G	ENSP00000430161.1:p.Trp122Gly
ENST00000522691.1:n.238T>G
ENST00000523756.5:c.4807T>G
NM_003235.4:c.8152T>G	NP_003226.4:p.Trp2718Gly
XM_005251038.3:c.7960T>G	XP_005251095.1:p.Trp2654Gly
XM_006716622.2:c.8089T>G	XP_006716685.1:p.Trp2697Gly
XM_005251038.4:c.7960T>G	XP_005251095.1:p.Trp2654Gly
XM_006716622.3:c.8089T>G	XP_006716685.1:p.Trp2697Gly
XM_017013793.1:c.8086T>G	XP_016869282.1:p.Trp2696Gly
XM_017013794.1:c.8017T>G	XP_016869283.1:p.Trp2673Gly
XM_017013795.1:c.7981T>G	XP_016869284.1:p.Trp2661Gly
XM_017013796.1:c.7933T>G	XP_016869285.1:p.Trp2645Gly
XM_017013797.1:c.7891T>G	XP_016869286.1:p.Trp2631Gly
NM_003235.5:c.8152T>G MANE Select	NP_003226.4:p.Trp2718Gly