Canonical Allele Identifier: CA372233890

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134030223T>G (hg19) ; chr8:g.133017978T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133017978T>G , CM000670.2:g.133017978T>G	GRCh38
NC_000008.10:g.134030223T>G , CM000670.1:g.134030223T>G	GRCh37
NC_000008.9:g.134099405T>G	NCBI36
NG_015832.1:g.156019T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6763T>G MANE Select	ENSP00000220616.4:p.Trp2255Gly
ENST00000220616.8:c.6763T>G	ENSP00000220616.4:p.Trp2255Gly
ENST00000518108.1:c.168+112T>G
ENST00000519178.5:c.2129T>G
ENST00000519543.5:c.1162T>G	ENSP00000430430.1:p.Trp388Gly
ENST00000523756.5:c.3418T>G
NM_003235.4:c.6763T>G	NP_003226.4:p.Trp2255Gly
XM_005251038.3:c.6571T>G	XP_005251095.1:p.Trp2191Gly
XM_006716622.2:c.6700T>G	XP_006716685.1:p.Trp2234Gly
XM_005251038.4:c.6571T>G	XP_005251095.1:p.Trp2191Gly
XM_006716622.3:c.6700T>G	XP_006716685.1:p.Trp2234Gly
XM_017013793.1:c.6697T>G	XP_016869282.1:p.Trp2233Gly
XM_017013794.1:c.6763T>G	XP_016869283.1:p.Trp2255Gly
XM_017013795.1:c.6592T>G	XP_016869284.1:p.Trp2198Gly
XM_017013796.1:c.6544T>G	XP_016869285.1:p.Trp2182Gly
XM_017013797.1:c.6502T>G	XP_016869286.1:p.Trp2168Gly
XM_017013798.1:c.6763T>G	XP_016869287.1:p.Trp2255Gly
NM_003235.5:c.6763T>G MANE Select	NP_003226.4:p.Trp2255Gly