Canonical Allele Identifier: CA463017030

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145750A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133506A>C , CM000670.2:g.133133506A>C	GRCh38
NC_000008.10:g.134145750A>C , CM000670.1:g.134145750A>C	GRCh37
NC_000008.9:g.134214932A>C	NCBI36
NG_015832.1:g.271546A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8034A>C MANE Select	ENSP00000220616.4:p.Val2678=
ENST00000220616.8:c.8034A>C	ENSP00000220616.4:p.Val2678=
ENST00000519178.5:c.3400A>C
ENST00000519543.5:c.2433A>C	ENSP00000430430.1:p.Val811=
ENST00000521107.1:c.246A>C	ENSP00000430161.1:p.Val82=
ENST00000522691.1:n.120A>C
ENST00000523756.5:c.4689A>C
NM_003235.4:c.8034A>C	NP_003226.4:p.Val2678=
XM_005251038.3:c.7842A>C	XP_005251095.1:p.Val2614=
XM_006716622.2:c.7971A>C	XP_006716685.1:p.Val2657=
XM_005251038.4:c.7842A>C	XP_005251095.1:p.Val2614=
XM_006716622.3:c.7971A>C	XP_006716685.1:p.Val2657=
XM_017013793.1:c.7968A>C	XP_016869282.1:p.Val2656=
XM_017013794.1:c.7899A>C	XP_016869283.1:p.Val2633=
XM_017013795.1:c.7863A>C	XP_016869284.1:p.Val2621=
XM_017013796.1:c.7815A>C	XP_016869285.1:p.Val2605=
XM_017013797.1:c.7773A>C	XP_016869286.1:p.Val2591=
NM_003235.5:c.8034A>C MANE Select	NP_003226.4:p.Val2678=