Canonical Allele Identifier: CA463012913

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.133984105T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132971860T>C , CM000670.2:g.132971860T>C	GRCh38
NC_000008.10:g.133984105T>C , CM000670.1:g.133984105T>C	GRCh37
NC_000008.9:g.134053287T>C	NCBI36
NG_015832.1:g.109901T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6042T>C MANE Select	ENSP00000220616.4:p.Val2014=
ENST00000220616.8:c.6042T>C	ENSP00000220616.4:p.Val2014=
ENST00000519178.5:c.1408T>C
ENST00000519294.5:n.34T>C
ENST00000519543.5:c.504T>C	ENSP00000430430.1:p.Val168=
ENST00000520089.5:n.151T>C
ENST00000520197.5:n.179T>C
ENST00000523756.5:c.2697T>C
ENST00000524151.5:n.10T>C
NM_003235.4:c.6042T>C	NP_003226.4:p.Val2014=
XM_005251038.3:c.5850T>C	XP_005251095.1:p.Val1950=
XM_005251040.3:c.6042T>C	XP_005251097.1:p.Val2014=
XM_005251042.3:c.6042T>C	XP_005251099.1:p.Val2014=
XM_005251043.3:c.6042T>C	XP_005251100.1:p.Val2014=
XM_006716622.2:c.6042T>C	XP_006716685.1:p.Val2014=
XM_005251038.4:c.5850T>C	XP_005251095.1:p.Val1950=
XM_005251040.4:c.6042T>C	XP_005251097.1:p.Val2014=
XM_005251042.4:c.6042T>C	XP_005251099.1:p.Val2014=
XM_006716622.3:c.6042T>C	XP_006716685.1:p.Val2014=
XM_017013793.1:c.5976T>C	XP_016869282.1:p.Val1992=
XM_017013794.1:c.6042T>C	XP_016869283.1:p.Val2014=
XM_017013795.1:c.5871T>C	XP_016869284.1:p.Val1957=
XM_017013796.1:c.5823T>C	XP_016869285.1:p.Val1941=
XM_017013797.1:c.5781T>C	XP_016869286.1:p.Val1927=
XM_017013798.1:c.6042T>C	XP_016869287.1:p.Val2014=
XM_017013799.1:c.6042T>C	XP_016869288.1:p.Val2014=
XM_017013800.1:c.6042T>C	XP_016869289.1:p.Val2014=
NM_003235.5:c.6042T>C MANE Select	NP_003226.4:p.Val2014=