Canonical Allele Identifier: CA372253367

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145813G>C (hg19) ; chr8:g.133133569G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133569G>C , CM000670.2:g.133133569G>C	GRCh38
NC_000008.10:g.134145813G>C , CM000670.1:g.134145813G>C	GRCh37
NC_000008.9:g.134214995G>C	NCBI36
NG_015832.1:g.271609G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8097G>C MANE Select	ENSP00000220616.4:p.Glu2699Asp
ENST00000220616.8:c.8097G>C	ENSP00000220616.4:p.Glu2699Asp
ENST00000519178.5:c.3463G>C
ENST00000519543.5:c.2496G>C	ENSP00000430430.1:p.Glu832Asp
ENST00000521107.1:c.309G>C	ENSP00000430161.1:p.Glu103Asp
ENST00000522691.1:n.183G>C
ENST00000523756.5:c.4752G>C
NM_003235.4:c.8097G>C	NP_003226.4:p.Glu2699Asp
XM_005251038.3:c.7905G>C	XP_005251095.1:p.Glu2635Asp
XM_006716622.2:c.8034G>C	XP_006716685.1:p.Glu2678Asp
XM_005251038.4:c.7905G>C	XP_005251095.1:p.Glu2635Asp
XM_006716622.3:c.8034G>C	XP_006716685.1:p.Glu2678Asp
XM_017013793.1:c.8031G>C	XP_016869282.1:p.Glu2677Asp
XM_017013794.1:c.7962G>C	XP_016869283.1:p.Glu2654Asp
XM_017013795.1:c.7926G>C	XP_016869284.1:p.Glu2642Asp
XM_017013796.1:c.7878G>C	XP_016869285.1:p.Glu2626Asp
XM_017013797.1:c.7836G>C	XP_016869286.1:p.Glu2612Asp
NM_003235.5:c.8097G>C MANE Select	NP_003226.4:p.Glu2699Asp