Canonical Allele Identifier: CA372253426

Gene: TG

Linked Data

• dbSNP Id: rs2130424370
• MyVariant Identifiers: chr8:g.134145829C>A (hg19) ; chr8:g.133133585C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133585C>A , CM000670.2:g.133133585C>A	GRCh38
NC_000008.10:g.134145829C>A , CM000670.1:g.134145829C>A	GRCh37
NC_000008.9:g.134215011C>A	NCBI36
NG_015832.1:g.271625C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8113C>A MANE Select	ENSP00000220616.4:p.Pro2705Thr
ENST00000220616.8:c.8113C>A	ENSP00000220616.4:p.Pro2705Thr
ENST00000519178.5:c.3479C>A
ENST00000519543.5:c.2512C>A	ENSP00000430430.1:p.Pro838Thr
ENST00000521107.1:c.325C>A	ENSP00000430161.1:p.Pro109Thr
ENST00000522691.1:n.199C>A
ENST00000523756.5:c.4768C>A
NM_003235.4:c.8113C>A	NP_003226.4:p.Pro2705Thr
XM_005251038.3:c.7921C>A	XP_005251095.1:p.Pro2641Thr
XM_006716622.2:c.8050C>A	XP_006716685.1:p.Pro2684Thr
XM_005251038.4:c.7921C>A	XP_005251095.1:p.Pro2641Thr
XM_006716622.3:c.8050C>A	XP_006716685.1:p.Pro2684Thr
XM_017013793.1:c.8047C>A	XP_016869282.1:p.Pro2683Thr
XM_017013794.1:c.7978C>A	XP_016869283.1:p.Pro2660Thr
XM_017013795.1:c.7942C>A	XP_016869284.1:p.Pro2648Thr
XM_017013796.1:c.7894C>A	XP_016869285.1:p.Pro2632Thr
XM_017013797.1:c.7852C>A	XP_016869286.1:p.Pro2618Thr
NM_003235.5:c.8113C>A MANE Select	NP_003226.4:p.Pro2705Thr