Canonical Allele Identifier: CA463017171

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145819T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133575T>C , CM000670.2:g.133133575T>C	GRCh38
NC_000008.10:g.134145819T>C , CM000670.1:g.134145819T>C	GRCh37
NC_000008.9:g.134215001T>C	NCBI36
NG_015832.1:g.271615T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8103T>C MANE Select	ENSP00000220616.4:p.Ser2701=
ENST00000220616.8:c.8103T>C	ENSP00000220616.4:p.Ser2701=
ENST00000519178.5:c.3469T>C
ENST00000519543.5:c.2502T>C	ENSP00000430430.1:p.Ser834=
ENST00000521107.1:c.315T>C	ENSP00000430161.1:p.Ser105=
ENST00000522691.1:n.189T>C
ENST00000523756.5:c.4758T>C
NM_003235.4:c.8103T>C	NP_003226.4:p.Ser2701=
XM_005251038.3:c.7911T>C	XP_005251095.1:p.Ser2637=
XM_006716622.2:c.8040T>C	XP_006716685.1:p.Ser2680=
XM_005251038.4:c.7911T>C	XP_005251095.1:p.Ser2637=
XM_006716622.3:c.8040T>C	XP_006716685.1:p.Ser2680=
XM_017013793.1:c.8037T>C	XP_016869282.1:p.Ser2679=
XM_017013794.1:c.7968T>C	XP_016869283.1:p.Ser2656=
XM_017013795.1:c.7932T>C	XP_016869284.1:p.Ser2644=
XM_017013796.1:c.7884T>C	XP_016869285.1:p.Ser2628=
XM_017013797.1:c.7842T>C	XP_016869286.1:p.Ser2614=
NM_003235.5:c.8103T>C MANE Select	NP_003226.4:p.Ser2701=