Canonical Allele Identifier: CA372253682

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145893A>C (hg19) ; chr8:g.133133649A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133649A>C , CM000670.2:g.133133649A>C	GRCh38
NC_000008.10:g.134145893A>C , CM000670.1:g.134145893A>C	GRCh37
NC_000008.9:g.134215075A>C	NCBI36
NG_015832.1:g.271689A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8177A>C MANE Select	ENSP00000220616.4:p.Lys2726Thr
ENST00000220616.8:c.8177A>C	ENSP00000220616.4:p.Lys2726Thr
ENST00000519178.5:c.3543A>C
ENST00000519543.5:c.2576A>C	ENSP00000430430.1:p.Lys859Thr
ENST00000521107.1:c.389A>C	ENSP00000430161.1:p.Lys130Thr
ENST00000522691.1:n.263A>C
ENST00000523756.5:c.4832A>C
NM_003235.4:c.8177A>C	NP_003226.4:p.Lys2726Thr
XM_005251038.3:c.7985A>C	XP_005251095.1:p.Lys2662Thr
XM_006716622.2:c.8114A>C	XP_006716685.1:p.Lys2705Thr
XM_005251038.4:c.7985A>C	XP_005251095.1:p.Lys2662Thr
XM_006716622.3:c.8114A>C	XP_006716685.1:p.Lys2705Thr
XM_017013793.1:c.8111A>C	XP_016869282.1:p.Lys2704Thr
XM_017013794.1:c.8042A>C	XP_016869283.1:p.Lys2681Thr
XM_017013795.1:c.8006A>C	XP_016869284.1:p.Lys2669Thr
XM_017013796.1:c.7958A>C	XP_016869285.1:p.Lys2653Thr
XM_017013797.1:c.7916A>C	XP_016869286.1:p.Lys2639Thr
NM_003235.5:c.8177A>C MANE Select	NP_003226.4:p.Lys2726Thr