Canonical Allele Identifier: CA372253648

Gene: TG

Linked Data

• dbSNP Id: rs1174442850
• gnomAD v2: 8-134145881-T-C
• MyVariant Identifiers: chr8:g.134145881T>C (hg19) ; chr8:g.133133637T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133637T>C , CM000670.2:g.133133637T>C	GRCh38
NC_000008.10:g.134145881T>C , CM000670.1:g.134145881T>C	GRCh37
NC_000008.9:g.134215063T>C	NCBI36
NG_015832.1:g.271677T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8165T>C MANE Select	ENSP00000220616.4:p.Ile2722Thr
ENST00000220616.8:c.8165T>C	ENSP00000220616.4:p.Ile2722Thr
ENST00000519178.5:c.3531T>C
ENST00000519543.5:c.2564T>C	ENSP00000430430.1:p.Ile855Thr
ENST00000521107.1:c.377T>C	ENSP00000430161.1:p.Ile126Thr
ENST00000522691.1:n.251T>C
ENST00000523756.5:c.4820T>C
NM_003235.4:c.8165T>C	NP_003226.4:p.Ile2722Thr
XM_005251038.3:c.7973T>C	XP_005251095.1:p.Ile2658Thr
XM_006716622.2:c.8102T>C	XP_006716685.1:p.Ile2701Thr
XM_005251038.4:c.7973T>C	XP_005251095.1:p.Ile2658Thr
XM_006716622.3:c.8102T>C	XP_006716685.1:p.Ile2701Thr
XM_017013793.1:c.8099T>C	XP_016869282.1:p.Ile2700Thr
XM_017013794.1:c.8030T>C	XP_016869283.1:p.Ile2677Thr
XM_017013795.1:c.7994T>C	XP_016869284.1:p.Ile2665Thr
XM_017013796.1:c.7946T>C	XP_016869285.1:p.Ile2649Thr
XM_017013797.1:c.7904T>C	XP_016869286.1:p.Ile2635Thr
NM_003235.5:c.8165T>C MANE Select	NP_003226.4:p.Ile2722Thr