Canonical Allele Identifier: CA372233868

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134030213G>A (hg19) ; chr8:g.133017968G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133017968G>A , CM000670.2:g.133017968G>A	GRCh38
NC_000008.10:g.134030213G>A , CM000670.1:g.134030213G>A	GRCh37
NC_000008.9:g.134099395G>A	NCBI36
NG_015832.1:g.156009G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6753G>A MANE Select	ENSP00000220616.4:p.Trp2251Ter
ENST00000220616.8:c.6753G>A	ENSP00000220616.4:p.Trp2251Ter
ENST00000518108.1:c.168+102G>A
ENST00000519178.5:c.2119G>A
ENST00000519543.5:c.1152G>A	ENSP00000430430.1:p.Trp384Ter
ENST00000523756.5:c.3408G>A
NM_003235.4:c.6753G>A	NP_003226.4:p.Trp2251Ter
XM_005251038.3:c.6561G>A	XP_005251095.1:p.Trp2187Ter
XM_006716622.2:c.6690G>A	XP_006716685.1:p.Trp2230Ter
XM_005251038.4:c.6561G>A	XP_005251095.1:p.Trp2187Ter
XM_006716622.3:c.6690G>A	XP_006716685.1:p.Trp2230Ter
XM_017013793.1:c.6687G>A	XP_016869282.1:p.Trp2229Ter
XM_017013794.1:c.6753G>A	XP_016869283.1:p.Trp2251Ter
XM_017013795.1:c.6582G>A	XP_016869284.1:p.Trp2194Ter
XM_017013796.1:c.6534G>A	XP_016869285.1:p.Trp2178Ter
XM_017013797.1:c.6492G>A	XP_016869286.1:p.Trp2164Ter
XM_017013798.1:c.6753G>A	XP_016869287.1:p.Trp2251Ter
NM_003235.5:c.6753G>A MANE Select	NP_003226.4:p.Trp2251Ter