Canonical Allele Identifier: CA372253061

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145736T>G (hg19) ; chr8:g.133133492T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133492T>G , CM000670.2:g.133133492T>G	GRCh38
NC_000008.10:g.134145736T>G , CM000670.1:g.134145736T>G	GRCh37
NC_000008.9:g.134214918T>G	NCBI36
NG_015832.1:g.271532T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8020T>G MANE Select	ENSP00000220616.4:p.Phe2674Val
ENST00000220616.8:c.8020T>G	ENSP00000220616.4:p.Phe2674Val
ENST00000519178.5:c.3386T>G
ENST00000519543.5:c.2419T>G	ENSP00000430430.1:p.Phe807Val
ENST00000521107.1:c.232T>G	ENSP00000430161.1:p.Phe78Val
ENST00000522691.1:n.106T>G
ENST00000523756.5:c.4675T>G
NM_003235.4:c.8020T>G	NP_003226.4:p.Phe2674Val
XM_005251038.3:c.7828T>G	XP_005251095.1:p.Phe2610Val
XM_006716622.2:c.7957T>G	XP_006716685.1:p.Phe2653Val
XM_005251038.4:c.7828T>G	XP_005251095.1:p.Phe2610Val
XM_006716622.3:c.7957T>G	XP_006716685.1:p.Phe2653Val
XM_017013793.1:c.7954T>G	XP_016869282.1:p.Phe2652Val
XM_017013794.1:c.7885T>G	XP_016869283.1:p.Phe2629Val
XM_017013795.1:c.7849T>G	XP_016869284.1:p.Phe2617Val
XM_017013796.1:c.7801T>G	XP_016869285.1:p.Phe2601Val
XM_017013797.1:c.7759T>G	XP_016869286.1:p.Phe2587Val
NM_003235.5:c.8020T>G MANE Select	NP_003226.4:p.Phe2674Val