Canonical Allele Identifier: CA372236541

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.133984049T>G (hg19) ; chr8:g.132971804T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132971804T>G , CM000670.2:g.132971804T>G	GRCh38
NC_000008.10:g.133984049T>G , CM000670.1:g.133984049T>G	GRCh37
NC_000008.9:g.134053231T>G	NCBI36
NG_015832.1:g.109845T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000220616.9:c.5986T>G MANE Select	ENSP00000220616.4:p.Cys1996Gly
ENST00000220616.8:c.5986T>G	ENSP00000220616.4:p.Cys1996Gly
ENST00000519178.5:c.1352T>G
ENST00000519543.5:c.448T>G	ENSP00000430430.1:p.Cys150Gly
ENST00000520089.5:n.95T>G
ENST00000520197.5:n.123T>G
ENST00000523756.5:c.2641T>G
NM_003235.4:c.5986T>G	NP_003226.4:p.Cys1996Gly
XM_005251038.3:c.5794T>G	XP_005251095.1:p.Cys1932Gly
XM_005251040.3:c.5986T>G	XP_005251097.1:p.Cys1996Gly
XM_005251042.3:c.5986T>G	XP_005251099.1:p.Cys1996Gly
XM_005251043.3:c.5986T>G	XP_005251100.1:p.Cys1996Gly
XM_006716622.2:c.5986T>G	XP_006716685.1:p.Cys1996Gly
XM_005251038.4:c.5794T>G	XP_005251095.1:p.Cys1932Gly
XM_005251040.4:c.5986T>G	XP_005251097.1:p.Cys1996Gly
XM_005251042.4:c.5986T>G	XP_005251099.1:p.Cys1996Gly
XM_006716622.3:c.5986T>G	XP_006716685.1:p.Cys1996Gly
XM_017013793.1:c.5920T>G	XP_016869282.1:p.Cys1974Gly
XM_017013794.1:c.5986T>G	XP_016869283.1:p.Cys1996Gly
XM_017013795.1:c.5815T>G	XP_016869284.1:p.Cys1939Gly
XM_017013796.1:c.5767T>G	XP_016869285.1:p.Cys1923Gly
XM_017013797.1:c.5725T>G	XP_016869286.1:p.Cys1909Gly
XM_017013798.1:c.5986T>G	XP_016869287.1:p.Cys1996Gly
XM_017013799.1:c.5986T>G	XP_016869288.1:p.Cys1996Gly
XM_017013800.1:c.5986T>G	XP_016869289.1:p.Cys1996Gly
NM_003235.5:c.5986T>G MANE Select	NP_003226.4:p.Cys1996Gly