Canonical Allele Identifier: CA372253455

Gene: TG

Linked Data

• gnomAD v4: 8-133133592-G-T
• MyVariant Identifiers: chr8:g.134145836G>T (hg19) ; chr8:g.133133592G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133592G>T , CM000670.2:g.133133592G>T	GRCh38
NC_000008.10:g.134145836G>T , CM000670.1:g.134145836G>T	GRCh37
NC_000008.9:g.134215018G>T	NCBI36
NG_015832.1:g.271632G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8120G>T MANE Select	ENSP00000220616.4:p.Arg2707Leu
ENST00000220616.8:c.8120G>T	ENSP00000220616.4:p.Arg2707Leu
ENST00000519178.5:c.3486G>T
ENST00000519543.5:c.2519G>T	ENSP00000430430.1:p.Arg840Leu
ENST00000521107.1:c.332G>T	ENSP00000430161.1:p.Arg111Leu
ENST00000522691.1:n.206G>T
ENST00000523756.5:c.4775G>T
NM_003235.4:c.8120G>T	NP_003226.4:p.Arg2707Leu
XM_005251038.3:c.7928G>T	XP_005251095.1:p.Arg2643Leu
XM_006716622.2:c.8057G>T	XP_006716685.1:p.Arg2686Leu
XM_005251038.4:c.7928G>T	XP_005251095.1:p.Arg2643Leu
XM_006716622.3:c.8057G>T	XP_006716685.1:p.Arg2686Leu
XM_017013793.1:c.8054G>T	XP_016869282.1:p.Arg2685Leu
XM_017013794.1:c.7985G>T	XP_016869283.1:p.Arg2662Leu
XM_017013795.1:c.7949G>T	XP_016869284.1:p.Arg2650Leu
XM_017013796.1:c.7901G>T	XP_016869285.1:p.Arg2634Leu
XM_017013797.1:c.7859G>T	XP_016869286.1:p.Arg2620Leu
NM_003235.5:c.8120G>T MANE Select	NP_003226.4:p.Arg2707Leu