Canonical Allele Identifier: CA372253291

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145797G>C (hg19) ; chr8:g.133133553G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133553G>C , CM000670.2:g.133133553G>C	GRCh38
NC_000008.10:g.134145797G>C , CM000670.1:g.134145797G>C	GRCh37
NC_000008.9:g.134214979G>C	NCBI36
NG_015832.1:g.271593G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8081G>C MANE Select	ENSP00000220616.4:p.Gly2694Ala
ENST00000220616.8:c.8081G>C	ENSP00000220616.4:p.Gly2694Ala
ENST00000519178.5:c.3447G>C
ENST00000519543.5:c.2480G>C	ENSP00000430430.1:p.Gly827Ala
ENST00000521107.1:c.293G>C	ENSP00000430161.1:p.Gly98Ala
ENST00000522691.1:n.167G>C
ENST00000523756.5:c.4736G>C
NM_003235.4:c.8081G>C	NP_003226.4:p.Gly2694Ala
XM_005251038.3:c.7889G>C	XP_005251095.1:p.Gly2630Ala
XM_006716622.2:c.8018G>C	XP_006716685.1:p.Gly2673Ala
XM_005251038.4:c.7889G>C	XP_005251095.1:p.Gly2630Ala
XM_006716622.3:c.8018G>C	XP_006716685.1:p.Gly2673Ala
XM_017013793.1:c.8015G>C	XP_016869282.1:p.Gly2672Ala
XM_017013794.1:c.7946G>C	XP_016869283.1:p.Gly2649Ala
XM_017013795.1:c.7910G>C	XP_016869284.1:p.Gly2637Ala
XM_017013796.1:c.7862G>C	XP_016869285.1:p.Gly2621Ala
XM_017013797.1:c.7820G>C	XP_016869286.1:p.Gly2607Ala
NM_003235.5:c.8081G>C MANE Select	NP_003226.4:p.Gly2694Ala