Canonical Allele Identifier: CA372252974

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145716A>T (hg19) ; chr8:g.133133472A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133472A>T , CM000670.2:g.133133472A>T	GRCh38
NC_000008.10:g.134145716A>T , CM000670.1:g.134145716A>T	GRCh37
NC_000008.9:g.134214898A>T	NCBI36
NG_015832.1:g.271512A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8000A>T MANE Select	ENSP00000220616.4:p.Asn2667Ile
ENST00000220616.8:c.8000A>T	ENSP00000220616.4:p.Asn2667Ile
ENST00000519178.5:c.3366A>T
ENST00000519543.5:c.2399A>T	ENSP00000430430.1:p.Asn800Ile
ENST00000521107.1:c.212A>T	ENSP00000430161.1:p.Asn71Ile
ENST00000522691.1:n.86A>T
ENST00000523756.5:c.4655A>T
NM_003235.4:c.8000A>T	NP_003226.4:p.Asn2667Ile
XM_005251038.3:c.7808A>T	XP_005251095.1:p.Asn2603Ile
XM_006716622.2:c.7937A>T	XP_006716685.1:p.Asn2646Ile
XM_005251038.4:c.7808A>T	XP_005251095.1:p.Asn2603Ile
XM_006716622.3:c.7937A>T	XP_006716685.1:p.Asn2646Ile
XM_017013793.1:c.7934A>T	XP_016869282.1:p.Asn2645Ile
XM_017013794.1:c.7865A>T	XP_016869283.1:p.Asn2622Ile
XM_017013795.1:c.7829A>T	XP_016869284.1:p.Asn2610Ile
XM_017013796.1:c.7781A>T	XP_016869285.1:p.Asn2594Ile
XM_017013797.1:c.7739A>T	XP_016869286.1:p.Asn2580Ile
NM_003235.5:c.8000A>T MANE Select	NP_003226.4:p.Asn2667Ile