Canonical Allele Identifier: CA372253167

Gene: TG

Linked Data

• dbSNP Id: rs1377662259
• gnomAD v2: 8-134145764-C-G
• gnomAD v4: 8-133133520-C-G
• MyVariant Identifiers: chr8:g.134145764C>G (hg19) ; chr8:g.133133520C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133520C>G , CM000670.2:g.133133520C>G	GRCh38
NC_000008.10:g.134145764C>G , CM000670.1:g.134145764C>G	GRCh37
NC_000008.9:g.134214946C>G	NCBI36
NG_015832.1:g.271560C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8048C>G MANE Select	ENSP00000220616.4:p.Thr2683Ser
ENST00000220616.8:c.8048C>G	ENSP00000220616.4:p.Thr2683Ser
ENST00000519178.5:c.3414C>G
ENST00000519543.5:c.2447C>G	ENSP00000430430.1:p.Thr816Ser
ENST00000521107.1:c.260C>G	ENSP00000430161.1:p.Thr87Ser
ENST00000522691.1:n.134C>G
ENST00000523756.5:c.4703C>G
NM_003235.4:c.8048C>G	NP_003226.4:p.Thr2683Ser
XM_005251038.3:c.7856C>G	XP_005251095.1:p.Thr2619Ser
XM_006716622.2:c.7985C>G	XP_006716685.1:p.Thr2662Ser
XM_005251038.4:c.7856C>G	XP_005251095.1:p.Thr2619Ser
XM_006716622.3:c.7985C>G	XP_006716685.1:p.Thr2662Ser
XM_017013793.1:c.7982C>G	XP_016869282.1:p.Thr2661Ser
XM_017013794.1:c.7913C>G	XP_016869283.1:p.Thr2638Ser
XM_017013795.1:c.7877C>G	XP_016869284.1:p.Thr2626Ser
XM_017013796.1:c.7829C>G	XP_016869285.1:p.Thr2610Ser
XM_017013797.1:c.7787C>G	XP_016869286.1:p.Thr2596Ser
NM_003235.5:c.8048C>G MANE Select	NP_003226.4:p.Thr2683Ser