Canonical Allele Identifier: CA4885896

Gene: TG

Linked Data

• dbSNP Id: rs116299430
• ExAC: 8:134145833 A / G
• gnomAD v2: 8-134145833-A-G
• gnomAD v3: 8-133133589-A-G
• gnomAD v4: 8-133133589-A-G
• MyVariant Identifiers: chr8:g.134145833A>G (hg19) ; chr8:g.133133589A>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8117A>G MANE Select	ENSP00000220616.4:p.Asn2706Ser
ENST00000220616.8:c.8117A>G	ENSP00000220616.4:p.Asn2706Ser
ENST00000519178.5:c.3483A>G
ENST00000519543.5:c.2516A>G	ENSP00000430430.1:p.Asn839Ser
ENST00000521107.1:c.329A>G	ENSP00000430161.1:p.Asn110Ser
ENST00000522691.1:n.203A>G
ENST00000523756.5:c.4772A>G
NM_003235.4:c.8117A>G	NP_003226.4:p.Asn2706Ser
XM_005251038.3:c.7925A>G	XP_005251095.1:p.Asn2642Ser
XM_006716622.2:c.8054A>G	XP_006716685.1:p.Asn2685Ser
XM_005251038.4:c.7925A>G	XP_005251095.1:p.Asn2642Ser
XM_006716622.3:c.8054A>G	XP_006716685.1:p.Asn2685Ser
XM_017013793.1:c.8051A>G	XP_016869282.1:p.Asn2684Ser
XM_017013794.1:c.7982A>G	XP_016869283.1:p.Asn2661Ser
XM_017013795.1:c.7946A>G	XP_016869284.1:p.Asn2649Ser
XM_017013796.1:c.7898A>G	XP_016869285.1:p.Asn2633Ser
XM_017013797.1:c.7856A>G	XP_016869286.1:p.Asn2619Ser
NM_003235.5:c.8117A>G MANE Select	NP_003226.4:p.Asn2706Ser