Canonical Allele Identifier: CA372253548

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145860G>T (hg19) ; chr8:g.133133616G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133616G>T , CM000670.2:g.133133616G>T	GRCh38
NC_000008.10:g.134145860G>T , CM000670.1:g.134145860G>T	GRCh37
NC_000008.9:g.134215042G>T	NCBI36
NG_015832.1:g.271656G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8144G>T MANE Select	ENSP00000220616.4:p.Cys2715Phe
ENST00000220616.8:c.8144G>T	ENSP00000220616.4:p.Cys2715Phe
ENST00000519178.5:c.3510G>T
ENST00000519543.5:c.2543G>T	ENSP00000430430.1:p.Cys848Phe
ENST00000521107.1:c.356G>T	ENSP00000430161.1:p.Cys119Phe
ENST00000522691.1:n.230G>T
ENST00000523756.5:c.4799G>T
NM_003235.4:c.8144G>T	NP_003226.4:p.Cys2715Phe
XM_005251038.3:c.7952G>T	XP_005251095.1:p.Cys2651Phe
XM_006716622.2:c.8081G>T	XP_006716685.1:p.Cys2694Phe
XM_005251038.4:c.7952G>T	XP_005251095.1:p.Cys2651Phe
XM_006716622.3:c.8081G>T	XP_006716685.1:p.Cys2694Phe
XM_017013793.1:c.8078G>T	XP_016869282.1:p.Cys2693Phe
XM_017013794.1:c.8009G>T	XP_016869283.1:p.Cys2670Phe
XM_017013795.1:c.7973G>T	XP_016869284.1:p.Cys2658Phe
XM_017013796.1:c.7925G>T	XP_016869285.1:p.Cys2642Phe
XM_017013797.1:c.7883G>T	XP_016869286.1:p.Cys2628Phe
NM_003235.5:c.8144G>T MANE Select	NP_003226.4:p.Cys2715Phe