Canonical Allele Identifier: CA372253311

Gene: TG

Linked Data

• gnomAD v4: 8-133133559-A-C
• MyVariant Identifiers: chr8:g.134145803A>C (hg19) ; chr8:g.133133559A>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8087A>C MANE Select	ENSP00000220616.4:p.Asn2696Thr
ENST00000220616.8:c.8087A>C	ENSP00000220616.4:p.Asn2696Thr
ENST00000519178.5:c.3453A>C
ENST00000519543.5:c.2486A>C	ENSP00000430430.1:p.Asn829Thr
ENST00000521107.1:c.299A>C	ENSP00000430161.1:p.Asn100Thr
ENST00000522691.1:n.173A>C
ENST00000523756.5:c.4742A>C
NM_003235.4:c.8087A>C	NP_003226.4:p.Asn2696Thr
XM_005251038.3:c.7895A>C	XP_005251095.1:p.Asn2632Thr
XM_006716622.2:c.8024A>C	XP_006716685.1:p.Asn2675Thr
XM_005251038.4:c.7895A>C	XP_005251095.1:p.Asn2632Thr
XM_006716622.3:c.8024A>C	XP_006716685.1:p.Asn2675Thr
XM_017013793.1:c.8021A>C	XP_016869282.1:p.Asn2674Thr
XM_017013794.1:c.7952A>C	XP_016869283.1:p.Asn2651Thr
XM_017013795.1:c.7916A>C	XP_016869284.1:p.Asn2639Thr
XM_017013796.1:c.7868A>C	XP_016869285.1:p.Asn2623Thr
XM_017013797.1:c.7826A>C	XP_016869286.1:p.Asn2609Thr
NM_003235.5:c.8087A>C MANE Select	NP_003226.4:p.Asn2696Thr