Canonical Allele Identifier: CA372253379

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145815T>C (hg19) ; chr8:g.133133571T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133571T>C , CM000670.2:g.133133571T>C	GRCh38
NC_000008.10:g.134145815T>C , CM000670.1:g.134145815T>C	GRCh37
NC_000008.9:g.134214997T>C	NCBI36
NG_015832.1:g.271611T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8099T>C MANE Select	ENSP00000220616.4:p.Phe2700Ser
ENST00000220616.8:c.8099T>C	ENSP00000220616.4:p.Phe2700Ser
ENST00000519178.5:c.3465T>C
ENST00000519543.5:c.2498T>C	ENSP00000430430.1:p.Phe833Ser
ENST00000521107.1:c.311T>C	ENSP00000430161.1:p.Phe104Ser
ENST00000522691.1:n.185T>C
ENST00000523756.5:c.4754T>C
NM_003235.4:c.8099T>C	NP_003226.4:p.Phe2700Ser
XM_005251038.3:c.7907T>C	XP_005251095.1:p.Phe2636Ser
XM_006716622.2:c.8036T>C	XP_006716685.1:p.Phe2679Ser
XM_005251038.4:c.7907T>C	XP_005251095.1:p.Phe2636Ser
XM_006716622.3:c.8036T>C	XP_006716685.1:p.Phe2679Ser
XM_017013793.1:c.8033T>C	XP_016869282.1:p.Phe2678Ser
XM_017013794.1:c.7964T>C	XP_016869283.1:p.Phe2655Ser
XM_017013795.1:c.7928T>C	XP_016869284.1:p.Phe2643Ser
XM_017013796.1:c.7880T>C	XP_016869285.1:p.Phe2627Ser
XM_017013797.1:c.7838T>C	XP_016869286.1:p.Phe2613Ser
NM_003235.5:c.8099T>C MANE Select	NP_003226.4:p.Phe2700Ser