Canonical Allele Identifier: CA372253072

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145739T>G (hg19) ; chr8:g.133133495T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133495T>G , CM000670.2:g.133133495T>G	GRCh38
NC_000008.10:g.134145739T>G , CM000670.1:g.134145739T>G	GRCh37
NC_000008.9:g.134214921T>G	NCBI36
NG_015832.1:g.271535T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8023T>G MANE Select	ENSP00000220616.4:p.Ser2675Ala
ENST00000220616.8:c.8023T>G	ENSP00000220616.4:p.Ser2675Ala
ENST00000519178.5:c.3389T>G
ENST00000519543.5:c.2422T>G	ENSP00000430430.1:p.Ser808Ala
ENST00000521107.1:c.235T>G	ENSP00000430161.1:p.Ser79Ala
ENST00000522691.1:n.109T>G
ENST00000523756.5:c.4678T>G
NM_003235.4:c.8023T>G	NP_003226.4:p.Ser2675Ala
XM_005251038.3:c.7831T>G	XP_005251095.1:p.Ser2611Ala
XM_006716622.2:c.7960T>G	XP_006716685.1:p.Ser2654Ala
XM_005251038.4:c.7831T>G	XP_005251095.1:p.Ser2611Ala
XM_006716622.3:c.7960T>G	XP_006716685.1:p.Ser2654Ala
XM_017013793.1:c.7957T>G	XP_016869282.1:p.Ser2653Ala
XM_017013794.1:c.7888T>G	XP_016869283.1:p.Ser2630Ala
XM_017013795.1:c.7852T>G	XP_016869284.1:p.Ser2618Ala
XM_017013796.1:c.7804T>G	XP_016869285.1:p.Ser2602Ala
XM_017013797.1:c.7762T>G	XP_016869286.1:p.Ser2588Ala
NM_003235.5:c.8023T>G MANE Select	NP_003226.4:p.Ser2675Ala