Canonical Allele Identifier: CA372253458

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145838C>G (hg19) ; chr8:g.133133594C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133594C>G , CM000670.2:g.133133594C>G	GRCh38
NC_000008.10:g.134145838C>G , CM000670.1:g.134145838C>G	GRCh37
NC_000008.9:g.134215020C>G	NCBI36
NG_015832.1:g.271634C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8122C>G MANE Select	ENSP00000220616.4:p.Gln2708Glu
ENST00000220616.8:c.8122C>G	ENSP00000220616.4:p.Gln2708Glu
ENST00000519178.5:c.3488C>G
ENST00000519543.5:c.2521C>G	ENSP00000430430.1:p.Gln841Glu
ENST00000521107.1:c.334C>G	ENSP00000430161.1:p.Gln112Glu
ENST00000522691.1:n.208C>G
ENST00000523756.5:c.4777C>G
NM_003235.4:c.8122C>G	NP_003226.4:p.Gln2708Glu
XM_005251038.3:c.7930C>G	XP_005251095.1:p.Gln2644Glu
XM_006716622.2:c.8059C>G	XP_006716685.1:p.Gln2687Glu
XM_005251038.4:c.7930C>G	XP_005251095.1:p.Gln2644Glu
XM_006716622.3:c.8059C>G	XP_006716685.1:p.Gln2687Glu
XM_017013793.1:c.8056C>G	XP_016869282.1:p.Gln2686Glu
XM_017013794.1:c.7987C>G	XP_016869283.1:p.Gln2663Glu
XM_017013795.1:c.7951C>G	XP_016869284.1:p.Gln2651Glu
XM_017013796.1:c.7903C>G	XP_016869285.1:p.Gln2635Glu
XM_017013797.1:c.7861C>G	XP_016869286.1:p.Gln2621Glu
NM_003235.5:c.8122C>G MANE Select	NP_003226.4:p.Gln2708Glu