Canonical Allele Identifier: CA372253453

Gene: TG

Linked Data

• dbSNP Id: rs143950166
• gnomAD v3: 8-133133592-G-C
• gnomAD v4: 8-133133592-G-C
• MyVariant Identifiers: chr8:g.134145836G>C (hg19) ; chr8:g.133133592G>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8120G>C MANE Select	ENSP00000220616.4:p.Arg2707Pro
ENST00000220616.8:c.8120G>C	ENSP00000220616.4:p.Arg2707Pro
ENST00000519178.5:c.3486G>C
ENST00000519543.5:c.2519G>C	ENSP00000430430.1:p.Arg840Pro
ENST00000521107.1:c.332G>C	ENSP00000430161.1:p.Arg111Pro
ENST00000522691.1:n.206G>C
ENST00000523756.5:c.4775G>C
NM_003235.4:c.8120G>C	NP_003226.4:p.Arg2707Pro
XM_005251038.3:c.7928G>C	XP_005251095.1:p.Arg2643Pro
XM_006716622.2:c.8057G>C	XP_006716685.1:p.Arg2686Pro
XM_005251038.4:c.7928G>C	XP_005251095.1:p.Arg2643Pro
XM_006716622.3:c.8057G>C	XP_006716685.1:p.Arg2686Pro
XM_017013793.1:c.8054G>C	XP_016869282.1:p.Arg2685Pro
XM_017013794.1:c.7985G>C	XP_016869283.1:p.Arg2662Pro
XM_017013795.1:c.7949G>C	XP_016869284.1:p.Arg2650Pro
XM_017013796.1:c.7901G>C	XP_016869285.1:p.Arg2634Pro
XM_017013797.1:c.7859G>C	XP_016869286.1:p.Arg2620Pro
NM_003235.5:c.8120G>C MANE Select	NP_003226.4:p.Arg2707Pro