Canonical Allele Identifier: CA372252968

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145715A>G (hg19) ; chr8:g.133133471A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133471A>G , CM000670.2:g.133133471A>G	GRCh38
NC_000008.10:g.134145715A>G , CM000670.1:g.134145715A>G	GRCh37
NC_000008.9:g.134214897A>G	NCBI36
NG_015832.1:g.271511A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.7999A>G MANE Select	ENSP00000220616.4:p.Asn2667Asp
ENST00000220616.8:c.7999A>G	ENSP00000220616.4:p.Asn2667Asp
ENST00000519178.5:c.3365A>G
ENST00000519543.5:c.2398A>G	ENSP00000430430.1:p.Asn800Asp
ENST00000521107.1:c.211A>G	ENSP00000430161.1:p.Asn71Asp
ENST00000522691.1:n.85A>G
ENST00000523756.5:c.4654A>G
NM_003235.4:c.7999A>G	NP_003226.4:p.Asn2667Asp
XM_005251038.3:c.7807A>G	XP_005251095.1:p.Asn2603Asp
XM_006716622.2:c.7936A>G	XP_006716685.1:p.Asn2646Asp
XM_005251038.4:c.7807A>G	XP_005251095.1:p.Asn2603Asp
XM_006716622.3:c.7936A>G	XP_006716685.1:p.Asn2646Asp
XM_017013793.1:c.7933A>G	XP_016869282.1:p.Asn2645Asp
XM_017013794.1:c.7864A>G	XP_016869283.1:p.Asn2622Asp
XM_017013795.1:c.7828A>G	XP_016869284.1:p.Asn2610Asp
XM_017013796.1:c.7780A>G	XP_016869285.1:p.Asn2594Asp
XM_017013797.1:c.7738A>G	XP_016869286.1:p.Asn2580Asp
NM_003235.5:c.7999A>G MANE Select	NP_003226.4:p.Asn2667Asp