Canonical Allele Identifier: CA372253252

Gene: TG

Linked Data

• gnomAD v4: 8-133133541-C-A
• MyVariant Identifiers: chr8:g.134145785C>A (hg19) ; chr8:g.133133541C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133541C>A , CM000670.2:g.133133541C>A	GRCh38
NC_000008.10:g.134145785C>A , CM000670.1:g.134145785C>A	GRCh37
NC_000008.9:g.134214967C>A	NCBI36
NG_015832.1:g.271581C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8069C>A MANE Select	ENSP00000220616.4:p.Pro2690His
ENST00000220616.8:c.8069C>A	ENSP00000220616.4:p.Pro2690His
ENST00000519178.5:c.3435C>A
ENST00000519543.5:c.2468C>A	ENSP00000430430.1:p.Pro823His
ENST00000521107.1:c.281C>A	ENSP00000430161.1:p.Pro94His
ENST00000522691.1:n.155C>A
ENST00000523756.5:c.4724C>A
NM_003235.4:c.8069C>A	NP_003226.4:p.Pro2690His
XM_005251038.3:c.7877C>A	XP_005251095.1:p.Pro2626His
XM_006716622.2:c.8006C>A	XP_006716685.1:p.Pro2669His
XM_005251038.4:c.7877C>A	XP_005251095.1:p.Pro2626His
XM_006716622.3:c.8006C>A	XP_006716685.1:p.Pro2669His
XM_017013793.1:c.8003C>A	XP_016869282.1:p.Pro2668His
XM_017013794.1:c.7934C>A	XP_016869283.1:p.Pro2645His
XM_017013795.1:c.7898C>A	XP_016869284.1:p.Pro2633His
XM_017013796.1:c.7850C>A	XP_016869285.1:p.Pro2617His
XM_017013797.1:c.7808C>A	XP_016869286.1:p.Pro2603His
NM_003235.5:c.8069C>A MANE Select	NP_003226.4:p.Pro2690His