Canonical Allele Identifier: CA372253146

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145758T>G (hg19) ; chr8:g.133133514T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133514T>G , CM000670.2:g.133133514T>G	GRCh38
NC_000008.10:g.134145758T>G , CM000670.1:g.134145758T>G	GRCh37
NC_000008.9:g.134214940T>G	NCBI36
NG_015832.1:g.271554T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8042T>G MANE Select	ENSP00000220616.4:p.Phe2681Cys
ENST00000220616.8:c.8042T>G	ENSP00000220616.4:p.Phe2681Cys
ENST00000519178.5:c.3408T>G
ENST00000519543.5:c.2441T>G	ENSP00000430430.1:p.Phe814Cys
ENST00000521107.1:c.254T>G	ENSP00000430161.1:p.Phe85Cys
ENST00000522691.1:n.128T>G
ENST00000523756.5:c.4697T>G
NM_003235.4:c.8042T>G	NP_003226.4:p.Phe2681Cys
XM_005251038.3:c.7850T>G	XP_005251095.1:p.Phe2617Cys
XM_006716622.2:c.7979T>G	XP_006716685.1:p.Phe2660Cys
XM_005251038.4:c.7850T>G	XP_005251095.1:p.Phe2617Cys
XM_006716622.3:c.7979T>G	XP_006716685.1:p.Phe2660Cys
XM_017013793.1:c.7976T>G	XP_016869282.1:p.Phe2659Cys
XM_017013794.1:c.7907T>G	XP_016869283.1:p.Phe2636Cys
XM_017013795.1:c.7871T>G	XP_016869284.1:p.Phe2624Cys
XM_017013796.1:c.7823T>G	XP_016869285.1:p.Phe2608Cys
XM_017013797.1:c.7781T>G	XP_016869286.1:p.Phe2594Cys
NM_003235.5:c.8042T>G MANE Select	NP_003226.4:p.Phe2681Cys