Canonical Allele Identifier: CA372253641

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145880A>T (hg19) ; chr8:g.133133636A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133636A>T , CM000670.2:g.133133636A>T	GRCh38
NC_000008.10:g.134145880A>T , CM000670.1:g.134145880A>T	GRCh37
NC_000008.9:g.134215062A>T	NCBI36
NG_015832.1:g.271676A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8164A>T MANE Select	ENSP00000220616.4:p.Ile2722Phe
ENST00000220616.8:c.8164A>T	ENSP00000220616.4:p.Ile2722Phe
ENST00000519178.5:c.3530A>T
ENST00000519543.5:c.2563A>T	ENSP00000430430.1:p.Ile855Phe
ENST00000521107.1:c.376A>T	ENSP00000430161.1:p.Ile126Phe
ENST00000522691.1:n.250A>T
ENST00000523756.5:c.4819A>T
NM_003235.4:c.8164A>T	NP_003226.4:p.Ile2722Phe
XM_005251038.3:c.7972A>T	XP_005251095.1:p.Ile2658Phe
XM_006716622.2:c.8101A>T	XP_006716685.1:p.Ile2701Phe
XM_005251038.4:c.7972A>T	XP_005251095.1:p.Ile2658Phe
XM_006716622.3:c.8101A>T	XP_006716685.1:p.Ile2701Phe
XM_017013793.1:c.8098A>T	XP_016869282.1:p.Ile2700Phe
XM_017013794.1:c.8029A>T	XP_016869283.1:p.Ile2677Phe
XM_017013795.1:c.7993A>T	XP_016869284.1:p.Ile2665Phe
XM_017013796.1:c.7945A>T	XP_016869285.1:p.Ile2649Phe
XM_017013797.1:c.7903A>T	XP_016869286.1:p.Ile2635Phe
NM_003235.5:c.8164A>T MANE Select	NP_003226.4:p.Ile2722Phe