Canonical Allele Identifier: CA372253568

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145865T>G (hg19) ; chr8:g.133133621T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133621T>G , CM000670.2:g.133133621T>G	GRCh38
NC_000008.10:g.134145865T>G , CM000670.1:g.134145865T>G	GRCh37
NC_000008.9:g.134215047T>G	NCBI36
NG_015832.1:g.271661T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8149T>G MANE Select	ENSP00000220616.4:p.Phe2717Val
ENST00000220616.8:c.8149T>G	ENSP00000220616.4:p.Phe2717Val
ENST00000519178.5:c.3515T>G
ENST00000519543.5:c.2548T>G	ENSP00000430430.1:p.Phe850Val
ENST00000521107.1:c.361T>G	ENSP00000430161.1:p.Phe121Val
ENST00000522691.1:n.235T>G
ENST00000523756.5:c.4804T>G
NM_003235.4:c.8149T>G	NP_003226.4:p.Phe2717Val
XM_005251038.3:c.7957T>G	XP_005251095.1:p.Phe2653Val
XM_006716622.2:c.8086T>G	XP_006716685.1:p.Phe2696Val
XM_005251038.4:c.7957T>G	XP_005251095.1:p.Phe2653Val
XM_006716622.3:c.8086T>G	XP_006716685.1:p.Phe2696Val
XM_017013793.1:c.8083T>G	XP_016869282.1:p.Phe2695Val
XM_017013794.1:c.8014T>G	XP_016869283.1:p.Phe2672Val
XM_017013795.1:c.7978T>G	XP_016869284.1:p.Phe2660Val
XM_017013796.1:c.7930T>G	XP_016869285.1:p.Phe2644Val
XM_017013797.1:c.7888T>G	XP_016869286.1:p.Phe2630Val
NM_003235.5:c.8149T>G MANE Select	NP_003226.4:p.Phe2717Val