Canonical Allele Identifier: CA372253496

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145848A>G (hg19) ; chr8:g.133133604A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133604A>G , CM000670.2:g.133133604A>G	GRCh38
NC_000008.10:g.134145848A>G , CM000670.1:g.134145848A>G	GRCh37
NC_000008.9:g.134215030A>G	NCBI36
NG_015832.1:g.271644A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8132A>G MANE Select	ENSP00000220616.4:p.Lys2711Arg
ENST00000220616.8:c.8132A>G	ENSP00000220616.4:p.Lys2711Arg
ENST00000519178.5:c.3498A>G
ENST00000519543.5:c.2531A>G	ENSP00000430430.1:p.Lys844Arg
ENST00000521107.1:c.344A>G	ENSP00000430161.1:p.Lys115Arg
ENST00000522691.1:n.218A>G
ENST00000523756.5:c.4787A>G
NM_003235.4:c.8132A>G	NP_003226.4:p.Lys2711Arg
XM_005251038.3:c.7940A>G	XP_005251095.1:p.Lys2647Arg
XM_006716622.2:c.8069A>G	XP_006716685.1:p.Lys2690Arg
XM_005251038.4:c.7940A>G	XP_005251095.1:p.Lys2647Arg
XM_006716622.3:c.8069A>G	XP_006716685.1:p.Lys2690Arg
XM_017013793.1:c.8066A>G	XP_016869282.1:p.Lys2689Arg
XM_017013794.1:c.7997A>G	XP_016869283.1:p.Lys2666Arg
XM_017013795.1:c.7961A>G	XP_016869284.1:p.Lys2654Arg
XM_017013796.1:c.7913A>G	XP_016869285.1:p.Lys2638Arg
XM_017013797.1:c.7871A>G	XP_016869286.1:p.Lys2624Arg
NM_003235.5:c.8132A>G MANE Select	NP_003226.4:p.Lys2711Arg