Canonical Allele Identifier: CA372253209

Gene: TG

Linked Data

• COSMIC: COSM749254
• MyVariant Identifiers: chr8:g.134145775G>C (hg19) ; chr8:g.133133531G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133531G>C , CM000670.2:g.133133531G>C	GRCh38
NC_000008.10:g.134145775G>C , CM000670.1:g.134145775G>C	GRCh37
NC_000008.9:g.134214957G>C	NCBI36
NG_015832.1:g.271571G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8059G>C MANE Select	ENSP00000220616.4:p.Asp2687His
ENST00000220616.8:c.8059G>C	ENSP00000220616.4:p.Asp2687His
ENST00000519178.5:c.3425G>C
ENST00000519543.5:c.2458G>C	ENSP00000430430.1:p.Asp820His
ENST00000521107.1:c.271G>C	ENSP00000430161.1:p.Asp91His
ENST00000522691.1:n.145G>C
ENST00000523756.5:c.4714G>C
NM_003235.4:c.8059G>C	NP_003226.4:p.Asp2687His
XM_005251038.3:c.7867G>C	XP_005251095.1:p.Asp2623His
XM_006716622.2:c.7996G>C	XP_006716685.1:p.Asp2666His
XM_005251038.4:c.7867G>C	XP_005251095.1:p.Asp2623His
XM_006716622.3:c.7996G>C	XP_006716685.1:p.Asp2666His
XM_017013793.1:c.7993G>C	XP_016869282.1:p.Asp2665His
XM_017013794.1:c.7924G>C	XP_016869283.1:p.Asp2642His
XM_017013795.1:c.7888G>C	XP_016869284.1:p.Asp2630His
XM_017013796.1:c.7840G>C	XP_016869285.1:p.Asp2614His
XM_017013797.1:c.7798G>C	XP_016869286.1:p.Asp2600His
NM_003235.5:c.8059G>C MANE Select	NP_003226.4:p.Asp2687His