Canonical Allele Identifier: CA372253526

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145854C>G (hg19) ; chr8:g.133133610C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133610C>G , CM000670.2:g.133133610C>G	GRCh38
NC_000008.10:g.134145854C>G , CM000670.1:g.134145854C>G	GRCh37
NC_000008.9:g.134215036C>G	NCBI36
NG_015832.1:g.271650C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8138C>G MANE Select	ENSP00000220616.4:p.Ala2713Gly
ENST00000220616.8:c.8138C>G	ENSP00000220616.4:p.Ala2713Gly
ENST00000519178.5:c.3504C>G
ENST00000519543.5:c.2537C>G	ENSP00000430430.1:p.Ala846Gly
ENST00000521107.1:c.350C>G	ENSP00000430161.1:p.Ala117Gly
ENST00000522691.1:n.224C>G
ENST00000523756.5:c.4793C>G
NM_003235.4:c.8138C>G	NP_003226.4:p.Ala2713Gly
XM_005251038.3:c.7946C>G	XP_005251095.1:p.Ala2649Gly
XM_006716622.2:c.8075C>G	XP_006716685.1:p.Ala2692Gly
XM_005251038.4:c.7946C>G	XP_005251095.1:p.Ala2649Gly
XM_006716622.3:c.8075C>G	XP_006716685.1:p.Ala2692Gly
XM_017013793.1:c.8072C>G	XP_016869282.1:p.Ala2691Gly
XM_017013794.1:c.8003C>G	XP_016869283.1:p.Ala2668Gly
XM_017013795.1:c.7967C>G	XP_016869284.1:p.Ala2656Gly
XM_017013796.1:c.7919C>G	XP_016869285.1:p.Ala2640Gly
XM_017013797.1:c.7877C>G	XP_016869286.1:p.Ala2626Gly
NM_003235.5:c.8138C>G MANE Select	NP_003226.4:p.Ala2713Gly