Canonical Allele Identifier: CA372253387

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145817A>T (hg19) ; chr8:g.133133573A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133573A>T , CM000670.2:g.133133573A>T	GRCh38
NC_000008.10:g.134145817A>T , CM000670.1:g.134145817A>T	GRCh37
NC_000008.9:g.134214999A>T	NCBI36
NG_015832.1:g.271613A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8101A>T MANE Select	ENSP00000220616.4:p.Ser2701Cys
ENST00000220616.8:c.8101A>T	ENSP00000220616.4:p.Ser2701Cys
ENST00000519178.5:c.3467A>T
ENST00000519543.5:c.2500A>T	ENSP00000430430.1:p.Ser834Cys
ENST00000521107.1:c.313A>T	ENSP00000430161.1:p.Ser105Cys
ENST00000522691.1:n.187A>T
ENST00000523756.5:c.4756A>T
NM_003235.4:c.8101A>T	NP_003226.4:p.Ser2701Cys
XM_005251038.3:c.7909A>T	XP_005251095.1:p.Ser2637Cys
XM_006716622.2:c.8038A>T	XP_006716685.1:p.Ser2680Cys
XM_005251038.4:c.7909A>T	XP_005251095.1:p.Ser2637Cys
XM_006716622.3:c.8038A>T	XP_006716685.1:p.Ser2680Cys
XM_017013793.1:c.8035A>T	XP_016869282.1:p.Ser2679Cys
XM_017013794.1:c.7966A>T	XP_016869283.1:p.Ser2656Cys
XM_017013795.1:c.7930A>T	XP_016869284.1:p.Ser2644Cys
XM_017013796.1:c.7882A>T	XP_016869285.1:p.Ser2628Cys
XM_017013797.1:c.7840A>T	XP_016869286.1:p.Ser2614Cys
NM_003235.5:c.8101A>T MANE Select	NP_003226.4:p.Ser2701Cys