Canonical Allele Identifier: CA372253444

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145833A>T (hg19) ; chr8:g.133133589A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133589A>T , CM000670.2:g.133133589A>T	GRCh38
NC_000008.10:g.134145833A>T , CM000670.1:g.134145833A>T	GRCh37
NC_000008.9:g.134215015A>T	NCBI36
NG_015832.1:g.271629A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8117A>T MANE Select	ENSP00000220616.4:p.Asn2706Ile
ENST00000220616.8:c.8117A>T	ENSP00000220616.4:p.Asn2706Ile
ENST00000519178.5:c.3483A>T
ENST00000519543.5:c.2516A>T	ENSP00000430430.1:p.Asn839Ile
ENST00000521107.1:c.329A>T	ENSP00000430161.1:p.Asn110Ile
ENST00000522691.1:n.203A>T
ENST00000523756.5:c.4772A>T
NM_003235.4:c.8117A>T	NP_003226.4:p.Asn2706Ile
XM_005251038.3:c.7925A>T	XP_005251095.1:p.Asn2642Ile
XM_006716622.2:c.8054A>T	XP_006716685.1:p.Asn2685Ile
XM_005251038.4:c.7925A>T	XP_005251095.1:p.Asn2642Ile
XM_006716622.3:c.8054A>T	XP_006716685.1:p.Asn2685Ile
XM_017013793.1:c.8051A>T	XP_016869282.1:p.Asn2684Ile
XM_017013794.1:c.7982A>T	XP_016869283.1:p.Asn2661Ile
XM_017013795.1:c.7946A>T	XP_016869284.1:p.Asn2649Ile
XM_017013796.1:c.7898A>T	XP_016869285.1:p.Asn2633Ile
XM_017013797.1:c.7856A>T	XP_016869286.1:p.Asn2619Ile
NM_003235.5:c.8117A>T MANE Select	NP_003226.4:p.Asn2706Ile