Canonical Allele Identifier: CA372253670

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145887C>A (hg19) ; chr8:g.133133643C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133643C>A , CM000670.2:g.133133643C>A	GRCh38
NC_000008.10:g.134145887C>A , CM000670.1:g.134145887C>A	GRCh37
NC_000008.9:g.134215069C>A	NCBI36
NG_015832.1:g.271683C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8171C>A MANE Select	ENSP00000220616.4:p.Ser2724Tyr
ENST00000220616.8:c.8171C>A	ENSP00000220616.4:p.Ser2724Tyr
ENST00000519178.5:c.3537C>A
ENST00000519543.5:c.2570C>A	ENSP00000430430.1:p.Ser857Tyr
ENST00000521107.1:c.383C>A	ENSP00000430161.1:p.Ser128Tyr
ENST00000522691.1:n.257C>A
ENST00000523756.5:c.4826C>A
NM_003235.4:c.8171C>A	NP_003226.4:p.Ser2724Tyr
XM_005251038.3:c.7979C>A	XP_005251095.1:p.Ser2660Tyr
XM_006716622.2:c.8108C>A	XP_006716685.1:p.Ser2703Tyr
XM_005251038.4:c.7979C>A	XP_005251095.1:p.Ser2660Tyr
XM_006716622.3:c.8108C>A	XP_006716685.1:p.Ser2703Tyr
XM_017013793.1:c.8105C>A	XP_016869282.1:p.Ser2702Tyr
XM_017013794.1:c.8036C>A	XP_016869283.1:p.Ser2679Tyr
XM_017013795.1:c.8000C>A	XP_016869284.1:p.Ser2667Tyr
XM_017013796.1:c.7952C>A	XP_016869285.1:p.Ser2651Tyr
XM_017013797.1:c.7910C>A	XP_016869286.1:p.Ser2637Tyr
NM_003235.5:c.8171C>A MANE Select	NP_003226.4:p.Ser2724Tyr