Canonical Allele Identifier: CA372253307

Gene: TG

Linked Data

• dbSNP Id: rs1852109786
• gnomAD v4: 8-133133558-A-G
• MyVariant Identifiers: chr8:g.134145802A>G (hg19) ; chr8:g.133133558A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133558A>G , CM000670.2:g.133133558A>G	GRCh38
NC_000008.10:g.134145802A>G , CM000670.1:g.134145802A>G	GRCh37
NC_000008.9:g.134214984A>G	NCBI36
NG_015832.1:g.271598A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8086A>G MANE Select	ENSP00000220616.4:p.Asn2696Asp
ENST00000220616.8:c.8086A>G	ENSP00000220616.4:p.Asn2696Asp
ENST00000519178.5:c.3452A>G
ENST00000519543.5:c.2485A>G	ENSP00000430430.1:p.Asn829Asp
ENST00000521107.1:c.298A>G	ENSP00000430161.1:p.Asn100Asp
ENST00000522691.1:n.172A>G
ENST00000523756.5:c.4741A>G
NM_003235.4:c.8086A>G	NP_003226.4:p.Asn2696Asp
XM_005251038.3:c.7894A>G	XP_005251095.1:p.Asn2632Asp
XM_006716622.2:c.8023A>G	XP_006716685.1:p.Asn2675Asp
XM_005251038.4:c.7894A>G	XP_005251095.1:p.Asn2632Asp
XM_006716622.3:c.8023A>G	XP_006716685.1:p.Asn2675Asp
XM_017013793.1:c.8020A>G	XP_016869282.1:p.Asn2674Asp
XM_017013794.1:c.7951A>G	XP_016869283.1:p.Asn2651Asp
XM_017013795.1:c.7915A>G	XP_016869284.1:p.Asn2639Asp
XM_017013796.1:c.7867A>G	XP_016869285.1:p.Asn2623Asp
XM_017013797.1:c.7825A>G	XP_016869286.1:p.Asn2609Asp
NM_003235.5:c.8086A>G MANE Select	NP_003226.4:p.Asn2696Asp