Canonical Allele Identifier: CA372253588

Gene: TG

Linked Data

• dbSNP Id: rs1258721562
• gnomAD v2: 8-134145869-G-A
• gnomAD v4: 8-133133625-G-A
• MyVariant Identifiers: chr8:g.134145869G>A (hg19) ; chr8:g.133133625G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133625G>A , CM000670.2:g.133133625G>A	GRCh38
NC_000008.10:g.134145869G>A , CM000670.1:g.134145869G>A	GRCh37
NC_000008.9:g.134215051G>A	NCBI36
NG_015832.1:g.271665G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8153G>A MANE Select	ENSP00000220616.4:p.Trp2718Ter
ENST00000220616.8:c.8153G>A	ENSP00000220616.4:p.Trp2718Ter
ENST00000519178.5:c.3519G>A
ENST00000519543.5:c.2552G>A	ENSP00000430430.1:p.Trp851Ter
ENST00000521107.1:c.365G>A	ENSP00000430161.1:p.Trp122Ter
ENST00000522691.1:n.239G>A
ENST00000523756.5:c.4808G>A
NM_003235.4:c.8153G>A	NP_003226.4:p.Trp2718Ter
XM_005251038.3:c.7961G>A	XP_005251095.1:p.Trp2654Ter
XM_006716622.2:c.8090G>A	XP_006716685.1:p.Trp2697Ter
XM_005251038.4:c.7961G>A	XP_005251095.1:p.Trp2654Ter
XM_006716622.3:c.8090G>A	XP_006716685.1:p.Trp2697Ter
XM_017013793.1:c.8087G>A	XP_016869282.1:p.Trp2696Ter
XM_017013794.1:c.8018G>A	XP_016869283.1:p.Trp2673Ter
XM_017013795.1:c.7982G>A	XP_016869284.1:p.Trp2661Ter
XM_017013796.1:c.7934G>A	XP_016869285.1:p.Trp2645Ter
XM_017013797.1:c.7892G>A	XP_016869286.1:p.Trp2631Ter
NM_003235.5:c.8153G>A MANE Select	NP_003226.4:p.Trp2718Ter