Canonical Allele Identifier: CA372252978

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145717T>G (hg19) ; chr8:g.133133473T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133473T>G , CM000670.2:g.133133473T>G	GRCh38
NC_000008.10:g.134145717T>G , CM000670.1:g.134145717T>G	GRCh37
NC_000008.9:g.134214899T>G	NCBI36
NG_015832.1:g.271513T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8001T>G MANE Select	ENSP00000220616.4:p.Asn2667Lys
ENST00000220616.8:c.8001T>G	ENSP00000220616.4:p.Asn2667Lys
ENST00000519178.5:c.3367T>G
ENST00000519543.5:c.2400T>G	ENSP00000430430.1:p.Asn800Lys
ENST00000521107.1:c.213T>G	ENSP00000430161.1:p.Asn71Lys
ENST00000522691.1:n.87T>G
ENST00000523756.5:c.4656T>G
NM_003235.4:c.8001T>G	NP_003226.4:p.Asn2667Lys
XM_005251038.3:c.7809T>G	XP_005251095.1:p.Asn2603Lys
XM_006716622.2:c.7938T>G	XP_006716685.1:p.Asn2646Lys
XM_005251038.4:c.7809T>G	XP_005251095.1:p.Asn2603Lys
XM_006716622.3:c.7938T>G	XP_006716685.1:p.Asn2646Lys
XM_017013793.1:c.7935T>G	XP_016869282.1:p.Asn2645Lys
XM_017013794.1:c.7866T>G	XP_016869283.1:p.Asn2622Lys
XM_017013795.1:c.7830T>G	XP_016869284.1:p.Asn2610Lys
XM_017013796.1:c.7782T>G	XP_016869285.1:p.Asn2594Lys
XM_017013797.1:c.7740T>G	XP_016869286.1:p.Asn2580Lys
NM_003235.5:c.8001T>G MANE Select	NP_003226.4:p.Asn2667Lys