Canonical Allele Identifier: CA372253313

Gene: TG

Linked Data

• dbSNP Id: rs764816968
• MyVariant Identifiers: chr8:g.134145803A>G (hg19) ; chr8:g.133133559A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133559A>G , CM000670.2:g.133133559A>G	GRCh38
NC_000008.10:g.134145803A>G , CM000670.1:g.134145803A>G	GRCh37
NC_000008.9:g.134214985A>G	NCBI36
NG_015832.1:g.271599A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8087A>G MANE Select	ENSP00000220616.4:p.Asn2696Ser
ENST00000220616.8:c.8087A>G	ENSP00000220616.4:p.Asn2696Ser
ENST00000519178.5:c.3453A>G
ENST00000519543.5:c.2486A>G	ENSP00000430430.1:p.Asn829Ser
ENST00000521107.1:c.299A>G	ENSP00000430161.1:p.Asn100Ser
ENST00000522691.1:n.173A>G
ENST00000523756.5:c.4742A>G
NM_003235.4:c.8087A>G	NP_003226.4:p.Asn2696Ser
XM_005251038.3:c.7895A>G	XP_005251095.1:p.Asn2632Ser
XM_006716622.2:c.8024A>G	XP_006716685.1:p.Asn2675Ser
XM_005251038.4:c.7895A>G	XP_005251095.1:p.Asn2632Ser
XM_006716622.3:c.8024A>G	XP_006716685.1:p.Asn2675Ser
XM_017013793.1:c.8021A>G	XP_016869282.1:p.Asn2674Ser
XM_017013794.1:c.7952A>G	XP_016869283.1:p.Asn2651Ser
XM_017013795.1:c.7916A>G	XP_016869284.1:p.Asn2639Ser
XM_017013796.1:c.7868A>G	XP_016869285.1:p.Asn2623Ser
XM_017013797.1:c.7826A>G	XP_016869286.1:p.Asn2609Ser
NM_003235.5:c.8087A>G MANE Select	NP_003226.4:p.Asn2696Ser