Canonical Allele Identifier: CA372233884

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134030220T>A (hg19) ; chr8:g.133017975T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133017975T>A , CM000670.2:g.133017975T>A	GRCh38
NC_000008.10:g.134030220T>A , CM000670.1:g.134030220T>A	GRCh37
NC_000008.9:g.134099402T>A	NCBI36
NG_015832.1:g.156016T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6760T>A MANE Select	ENSP00000220616.4:p.Ser2254Thr
ENST00000220616.8:c.6760T>A	ENSP00000220616.4:p.Ser2254Thr
ENST00000518108.1:c.168+109T>A
ENST00000519178.5:c.2126T>A
ENST00000519543.5:c.1159T>A	ENSP00000430430.1:p.Ser387Thr
ENST00000523756.5:c.3415T>A
NM_003235.4:c.6760T>A	NP_003226.4:p.Ser2254Thr
XM_005251038.3:c.6568T>A	XP_005251095.1:p.Ser2190Thr
XM_006716622.2:c.6697T>A	XP_006716685.1:p.Ser2233Thr
XM_005251038.4:c.6568T>A	XP_005251095.1:p.Ser2190Thr
XM_006716622.3:c.6697T>A	XP_006716685.1:p.Ser2233Thr
XM_017013793.1:c.6694T>A	XP_016869282.1:p.Ser2232Thr
XM_017013794.1:c.6760T>A	XP_016869283.1:p.Ser2254Thr
XM_017013795.1:c.6589T>A	XP_016869284.1:p.Ser2197Thr
XM_017013796.1:c.6541T>A	XP_016869285.1:p.Ser2181Thr
XM_017013797.1:c.6499T>A	XP_016869286.1:p.Ser2167Thr
XM_017013798.1:c.6760T>A	XP_016869287.1:p.Ser2254Thr
NM_003235.5:c.6760T>A MANE Select	NP_003226.4:p.Ser2254Thr