Canonical Allele Identifier: CA372253643

Gene: TG

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8164A>C MANE Select	ENSP00000220616.4:p.Ile2722Leu
ENST00000220616.8:c.8164A>C	ENSP00000220616.4:p.Ile2722Leu
ENST00000519178.5:c.3530A>C
ENST00000519543.5:c.2563A>C	ENSP00000430430.1:p.Ile855Leu
ENST00000521107.1:c.376A>C	ENSP00000430161.1:p.Ile126Leu
ENST00000522691.1:n.250A>C
ENST00000523756.5:c.4819A>C
NM_003235.4:c.8164A>C	NP_003226.4:p.Ile2722Leu
XM_005251038.3:c.7972A>C	XP_005251095.1:p.Ile2658Leu
XM_006716622.2:c.8101A>C	XP_006716685.1:p.Ile2701Leu
XM_005251038.4:c.7972A>C	XP_005251095.1:p.Ile2658Leu
XM_006716622.3:c.8101A>C	XP_006716685.1:p.Ile2701Leu
XM_017013793.1:c.8098A>C	XP_016869282.1:p.Ile2700Leu
XM_017013794.1:c.8029A>C	XP_016869283.1:p.Ile2677Leu
XM_017013795.1:c.7993A>C	XP_016869284.1:p.Ile2665Leu
XM_017013796.1:c.7945A>C	XP_016869285.1:p.Ile2649Leu
XM_017013797.1:c.7903A>C	XP_016869286.1:p.Ile2635Leu
NM_003235.5:c.8164A>C MANE Select	NP_003226.4:p.Ile2722Leu