Canonical Allele Identifier: CA372253593

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145870G>C (hg19) ; chr8:g.133133626G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133626G>C , CM000670.2:g.133133626G>C	GRCh38
NC_000008.10:g.134145870G>C , CM000670.1:g.134145870G>C	GRCh37
NC_000008.9:g.134215052G>C	NCBI36
NG_015832.1:g.271666G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8154G>C MANE Select	ENSP00000220616.4:p.Trp2718Cys
ENST00000220616.8:c.8154G>C	ENSP00000220616.4:p.Trp2718Cys
ENST00000519178.5:c.3520G>C
ENST00000519543.5:c.2553G>C	ENSP00000430430.1:p.Trp851Cys
ENST00000521107.1:c.366G>C	ENSP00000430161.1:p.Trp122Cys
ENST00000522691.1:n.240G>C
ENST00000523756.5:c.4809G>C
NM_003235.4:c.8154G>C	NP_003226.4:p.Trp2718Cys
XM_005251038.3:c.7962G>C	XP_005251095.1:p.Trp2654Cys
XM_006716622.2:c.8091G>C	XP_006716685.1:p.Trp2697Cys
XM_005251038.4:c.7962G>C	XP_005251095.1:p.Trp2654Cys
XM_006716622.3:c.8091G>C	XP_006716685.1:p.Trp2697Cys
XM_017013793.1:c.8088G>C	XP_016869282.1:p.Trp2696Cys
XM_017013794.1:c.8019G>C	XP_016869283.1:p.Trp2673Cys
XM_017013795.1:c.7983G>C	XP_016869284.1:p.Trp2661Cys
XM_017013796.1:c.7935G>C	XP_016869285.1:p.Trp2645Cys
XM_017013797.1:c.7893G>C	XP_016869286.1:p.Trp2631Cys
NM_003235.5:c.8154G>C MANE Select	NP_003226.4:p.Trp2718Cys