Canonical Allele Identifier: CA372253044

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145733G>C (hg19) ; chr8:g.133133489G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133489G>C , CM000670.2:g.133133489G>C	GRCh38
NC_000008.10:g.134145733G>C , CM000670.1:g.134145733G>C	GRCh37
NC_000008.9:g.134214915G>C	NCBI36
NG_015832.1:g.271529G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8017G>C MANE Select	ENSP00000220616.4:p.Glu2673Gln
ENST00000220616.8:c.8017G>C	ENSP00000220616.4:p.Glu2673Gln
ENST00000519178.5:c.3383G>C
ENST00000519543.5:c.2416G>C	ENSP00000430430.1:p.Glu806Gln
ENST00000521107.1:c.229G>C	ENSP00000430161.1:p.Glu77Gln
ENST00000522691.1:n.103G>C
ENST00000523756.5:c.4672G>C
NM_003235.4:c.8017G>C	NP_003226.4:p.Glu2673Gln
XM_005251038.3:c.7825G>C	XP_005251095.1:p.Glu2609Gln
XM_006716622.2:c.7954G>C	XP_006716685.1:p.Glu2652Gln
XM_005251038.4:c.7825G>C	XP_005251095.1:p.Glu2609Gln
XM_006716622.3:c.7954G>C	XP_006716685.1:p.Glu2652Gln
XM_017013793.1:c.7951G>C	XP_016869282.1:p.Glu2651Gln
XM_017013794.1:c.7882G>C	XP_016869283.1:p.Glu2628Gln
XM_017013795.1:c.7846G>C	XP_016869284.1:p.Glu2616Gln
XM_017013796.1:c.7798G>C	XP_016869285.1:p.Glu2600Gln
XM_017013797.1:c.7756G>C	XP_016869286.1:p.Glu2586Gln
NM_003235.5:c.8017G>C MANE Select	NP_003226.4:p.Glu2673Gln