Canonical Allele Identifier: CA372253534

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145857A>G (hg19) ; chr8:g.133133613A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133613A>G , CM000670.2:g.133133613A>G	GRCh38
NC_000008.10:g.134145857A>G , CM000670.1:g.134145857A>G	GRCh37
NC_000008.9:g.134215039A>G	NCBI36
NG_015832.1:g.271653A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8141A>G MANE Select	ENSP00000220616.4:p.Asp2714Gly
ENST00000220616.8:c.8141A>G	ENSP00000220616.4:p.Asp2714Gly
ENST00000519178.5:c.3507A>G
ENST00000519543.5:c.2540A>G	ENSP00000430430.1:p.Asp847Gly
ENST00000521107.1:c.353A>G	ENSP00000430161.1:p.Asp118Gly
ENST00000522691.1:n.227A>G
ENST00000523756.5:c.4796A>G
NM_003235.4:c.8141A>G	NP_003226.4:p.Asp2714Gly
XM_005251038.3:c.7949A>G	XP_005251095.1:p.Asp2650Gly
XM_006716622.2:c.8078A>G	XP_006716685.1:p.Asp2693Gly
XM_005251038.4:c.7949A>G	XP_005251095.1:p.Asp2650Gly
XM_006716622.3:c.8078A>G	XP_006716685.1:p.Asp2693Gly
XM_017013793.1:c.8075A>G	XP_016869282.1:p.Asp2692Gly
XM_017013794.1:c.8006A>G	XP_016869283.1:p.Asp2669Gly
XM_017013795.1:c.7970A>G	XP_016869284.1:p.Asp2657Gly
XM_017013796.1:c.7922A>G	XP_016869285.1:p.Asp2641Gly
XM_017013797.1:c.7880A>G	XP_016869286.1:p.Asp2627Gly
NM_003235.5:c.8141A>G MANE Select	NP_003226.4:p.Asp2714Gly