Canonical Allele Identifier: CA372233837

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134030205T>G (hg19) ; chr8:g.133017960T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133017960T>G , CM000670.2:g.133017960T>G	GRCh38
NC_000008.10:g.134030205T>G , CM000670.1:g.134030205T>G	GRCh37
NC_000008.9:g.134099387T>G	NCBI36
NG_015832.1:g.156001T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6745T>G MANE Select	ENSP00000220616.4:p.Leu2249Val
ENST00000220616.8:c.6745T>G	ENSP00000220616.4:p.Leu2249Val
ENST00000518108.1:c.168+94T>G
ENST00000519178.5:c.2111T>G
ENST00000519543.5:c.1144T>G	ENSP00000430430.1:p.Leu382Val
ENST00000522523.5:n.806T>G
ENST00000523756.5:c.3400T>G
NM_003235.4:c.6745T>G	NP_003226.4:p.Leu2249Val
XM_005251038.3:c.6553T>G	XP_005251095.1:p.Leu2185Val
XM_006716622.2:c.6682T>G	XP_006716685.1:p.Leu2228Val
XM_005251038.4:c.6553T>G	XP_005251095.1:p.Leu2185Val
XM_006716622.3:c.6682T>G	XP_006716685.1:p.Leu2228Val
XM_017013793.1:c.6679T>G	XP_016869282.1:p.Leu2227Val
XM_017013794.1:c.6745T>G	XP_016869283.1:p.Leu2249Val
XM_017013795.1:c.6574T>G	XP_016869284.1:p.Leu2192Val
XM_017013796.1:c.6526T>G	XP_016869285.1:p.Leu2176Val
XM_017013797.1:c.6484T>G	XP_016869286.1:p.Leu2162Val
XM_017013798.1:c.6745T>G	XP_016869287.1:p.Leu2249Val
NM_003235.5:c.6745T>G MANE Select	NP_003226.4:p.Leu2249Val