Canonical Allele Identifier: CA372253542

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145859T>C (hg19) ; chr8:g.133133615T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133615T>C , CM000670.2:g.133133615T>C	GRCh38
NC_000008.10:g.134145859T>C , CM000670.1:g.134145859T>C	GRCh37
NC_000008.9:g.134215041T>C	NCBI36
NG_015832.1:g.271655T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8143T>C MANE Select	ENSP00000220616.4:p.Cys2715Arg
ENST00000220616.8:c.8143T>C	ENSP00000220616.4:p.Cys2715Arg
ENST00000519178.5:c.3509T>C
ENST00000519543.5:c.2542T>C	ENSP00000430430.1:p.Cys848Arg
ENST00000521107.1:c.355T>C	ENSP00000430161.1:p.Cys119Arg
ENST00000522691.1:n.229T>C
ENST00000523756.5:c.4798T>C
NM_003235.4:c.8143T>C	NP_003226.4:p.Cys2715Arg
XM_005251038.3:c.7951T>C	XP_005251095.1:p.Cys2651Arg
XM_006716622.2:c.8080T>C	XP_006716685.1:p.Cys2694Arg
XM_005251038.4:c.7951T>C	XP_005251095.1:p.Cys2651Arg
XM_006716622.3:c.8080T>C	XP_006716685.1:p.Cys2694Arg
XM_017013793.1:c.8077T>C	XP_016869282.1:p.Cys2693Arg
XM_017013794.1:c.8008T>C	XP_016869283.1:p.Cys2670Arg
XM_017013795.1:c.7972T>C	XP_016869284.1:p.Cys2658Arg
XM_017013796.1:c.7924T>C	XP_016869285.1:p.Cys2642Arg
XM_017013797.1:c.7882T>C	XP_016869286.1:p.Cys2628Arg
NM_003235.5:c.8143T>C MANE Select	NP_003226.4:p.Cys2715Arg