Canonical Allele Identifier: CA372253179

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145769T>C (hg19) ; chr8:g.133133525T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133525T>C , CM000670.2:g.133133525T>C	GRCh38
NC_000008.10:g.134145769T>C , CM000670.1:g.134145769T>C	GRCh37
NC_000008.9:g.134214951T>C	NCBI36
NG_015832.1:g.271565T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8053T>C MANE Select	ENSP00000220616.4:p.Trp2685Arg
ENST00000220616.8:c.8053T>C	ENSP00000220616.4:p.Trp2685Arg
ENST00000519178.5:c.3419T>C
ENST00000519543.5:c.2452T>C	ENSP00000430430.1:p.Trp818Arg
ENST00000521107.1:c.265T>C	ENSP00000430161.1:p.Trp89Arg
ENST00000522691.1:n.139T>C
ENST00000523756.5:c.4708T>C
NM_003235.4:c.8053T>C	NP_003226.4:p.Trp2685Arg
XM_005251038.3:c.7861T>C	XP_005251095.1:p.Trp2621Arg
XM_006716622.2:c.7990T>C	XP_006716685.1:p.Trp2664Arg
XM_005251038.4:c.7861T>C	XP_005251095.1:p.Trp2621Arg
XM_006716622.3:c.7990T>C	XP_006716685.1:p.Trp2664Arg
XM_017013793.1:c.7987T>C	XP_016869282.1:p.Trp2663Arg
XM_017013794.1:c.7918T>C	XP_016869283.1:p.Trp2640Arg
XM_017013795.1:c.7882T>C	XP_016869284.1:p.Trp2628Arg
XM_017013796.1:c.7834T>C	XP_016869285.1:p.Trp2612Arg
XM_017013797.1:c.7792T>C	XP_016869286.1:p.Trp2598Arg
NM_003235.5:c.8053T>C MANE Select	NP_003226.4:p.Trp2685Arg