Canonical Allele Identifier: CA372253386

Gene: TG

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8101A>C MANE Select	ENSP00000220616.4:p.Ser2701Arg
ENST00000220616.8:c.8101A>C	ENSP00000220616.4:p.Ser2701Arg
ENST00000519178.5:c.3467A>C
ENST00000519543.5:c.2500A>C	ENSP00000430430.1:p.Ser834Arg
ENST00000521107.1:c.313A>C	ENSP00000430161.1:p.Ser105Arg
ENST00000522691.1:n.187A>C
ENST00000523756.5:c.4756A>C
NM_003235.4:c.8101A>C	NP_003226.4:p.Ser2701Arg
XM_005251038.3:c.7909A>C	XP_005251095.1:p.Ser2637Arg
XM_006716622.2:c.8038A>C	XP_006716685.1:p.Ser2680Arg
XM_005251038.4:c.7909A>C	XP_005251095.1:p.Ser2637Arg
XM_006716622.3:c.8038A>C	XP_006716685.1:p.Ser2680Arg
XM_017013793.1:c.8035A>C	XP_016869282.1:p.Ser2679Arg
XM_017013794.1:c.7966A>C	XP_016869283.1:p.Ser2656Arg
XM_017013795.1:c.7930A>C	XP_016869284.1:p.Ser2644Arg
XM_017013796.1:c.7882A>C	XP_016869285.1:p.Ser2628Arg
XM_017013797.1:c.7840A>C	XP_016869286.1:p.Ser2614Arg
NM_003235.5:c.8101A>C MANE Select	NP_003226.4:p.Ser2701Arg