Canonical Allele Identifier: CA372253618

Gene: TG

Linked Data

• dbSNP Id: rs1588156748
• gnomAD v4: 8-133133631-A-C
• MyVariant Identifiers: chr8:g.134145875A>C (hg19) ; chr8:g.133133631A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133631A>C , CM000670.2:g.133133631A>C	GRCh38
NC_000008.10:g.134145875A>C , CM000670.1:g.134145875A>C	GRCh37
NC_000008.9:g.134215057A>C	NCBI36
NG_015832.1:g.271671A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8159A>C MANE Select	ENSP00000220616.4:p.Lys2720Thr
ENST00000220616.8:c.8159A>C	ENSP00000220616.4:p.Lys2720Thr
ENST00000519178.5:c.3525A>C
ENST00000519543.5:c.2558A>C	ENSP00000430430.1:p.Lys853Thr
ENST00000521107.1:c.371A>C	ENSP00000430161.1:p.Lys124Thr
ENST00000522691.1:n.245A>C
ENST00000523756.5:c.4814A>C
NM_003235.4:c.8159A>C	NP_003226.4:p.Lys2720Thr
XM_005251038.3:c.7967A>C	XP_005251095.1:p.Lys2656Thr
XM_006716622.2:c.8096A>C	XP_006716685.1:p.Lys2699Thr
XM_005251038.4:c.7967A>C	XP_005251095.1:p.Lys2656Thr
XM_006716622.3:c.8096A>C	XP_006716685.1:p.Lys2699Thr
XM_017013793.1:c.8093A>C	XP_016869282.1:p.Lys2698Thr
XM_017013794.1:c.8024A>C	XP_016869283.1:p.Lys2675Thr
XM_017013795.1:c.7988A>C	XP_016869284.1:p.Lys2663Thr
XM_017013796.1:c.7940A>C	XP_016869285.1:p.Lys2647Thr
XM_017013797.1:c.7898A>C	XP_016869286.1:p.Lys2633Thr
NM_003235.5:c.8159A>C MANE Select	NP_003226.4:p.Lys2720Thr