Canonical Allele Identifier: CA372233724

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134030187T>C (hg19) ; chr8:g.133017942T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133017942T>C , CM000670.2:g.133017942T>C	GRCh38
NC_000008.10:g.134030187T>C , CM000670.1:g.134030187T>C	GRCh37
NC_000008.9:g.134099369T>C	NCBI36
NG_015832.1:g.155983T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6727T>C MANE Select	ENSP00000220616.4:p.Phe2243Leu
ENST00000220616.8:c.6727T>C	ENSP00000220616.4:p.Phe2243Leu
ENST00000518108.1:c.168+76T>C
ENST00000519178.5:c.2093T>C
ENST00000519543.5:c.1126T>C	ENSP00000430430.1:p.Phe376Leu
ENST00000522523.5:n.788T>C
ENST00000523756.5:c.3382T>C
NM_003235.4:c.6727T>C	NP_003226.4:p.Phe2243Leu
XM_005251038.3:c.6535T>C	XP_005251095.1:p.Phe2179Leu
XM_006716622.2:c.6664T>C	XP_006716685.1:p.Phe2222Leu
XM_005251038.4:c.6535T>C	XP_005251095.1:p.Phe2179Leu
XM_006716622.3:c.6664T>C	XP_006716685.1:p.Phe2222Leu
XM_017013793.1:c.6661T>C	XP_016869282.1:p.Phe2221Leu
XM_017013794.1:c.6727T>C	XP_016869283.1:p.Phe2243Leu
XM_017013795.1:c.6556T>C	XP_016869284.1:p.Phe2186Leu
XM_017013796.1:c.6508T>C	XP_016869285.1:p.Phe2170Leu
XM_017013797.1:c.6466T>C	XP_016869286.1:p.Phe2156Leu
XM_017013798.1:c.6727T>C	XP_016869287.1:p.Phe2243Leu
NM_003235.5:c.6727T>C MANE Select	NP_003226.4:p.Phe2243Leu