Canonical Allele Identifier: CA463017248

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145864C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133620C>G , CM000670.2:g.133133620C>G	GRCh38
NC_000008.10:g.134145864C>G , CM000670.1:g.134145864C>G	GRCh37
NC_000008.9:g.134215046C>G	NCBI36
NG_015832.1:g.271660C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8148C>G MANE Select	ENSP00000220616.4:p.Ser2716=
ENST00000220616.8:c.8148C>G	ENSP00000220616.4:p.Ser2716=
ENST00000519178.5:c.3514C>G
ENST00000519543.5:c.2547C>G	ENSP00000430430.1:p.Ser849=
ENST00000521107.1:c.360C>G	ENSP00000430161.1:p.Ser120=
ENST00000522691.1:n.234C>G
ENST00000523756.5:c.4803C>G
NM_003235.4:c.8148C>G	NP_003226.4:p.Ser2716=
XM_005251038.3:c.7956C>G	XP_005251095.1:p.Ser2652=
XM_006716622.2:c.8085C>G	XP_006716685.1:p.Ser2695=
XM_005251038.4:c.7956C>G	XP_005251095.1:p.Ser2652=
XM_006716622.3:c.8085C>G	XP_006716685.1:p.Ser2695=
XM_017013793.1:c.8082C>G	XP_016869282.1:p.Ser2694=
XM_017013794.1:c.8013C>G	XP_016869283.1:p.Ser2671=
XM_017013795.1:c.7977C>G	XP_016869284.1:p.Ser2659=
XM_017013796.1:c.7929C>G	XP_016869285.1:p.Ser2643=
XM_017013797.1:c.7887C>G	XP_016869286.1:p.Ser2629=
NM_003235.5:c.8148C>G MANE Select	NP_003226.4:p.Ser2716=