Canonical Allele Identifier: CA463011589

Gene: TG

Linked Data

• ClinVar Variation Id: 2720395
• ClinVar RCV Id: RCV003554040
• dbSNP Id: rs1188814693
• gnomAD v2: 8-133920486-G-T
• gnomAD v4: 8-132908241-G-T
• MyVariant Identifiers: chr8:g.133920486G>T (hg19) ; chr8:g.132908241G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132908241G>T , CM000670.2:g.132908241G>T	GRCh38
NC_000008.10:g.133920486G>T , CM000670.1:g.133920486G>T	GRCh37
NC_000008.9:g.133989668G>T	NCBI36
NG_015832.1:g.46282G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.3903G>T MANE Select	ENSP00000220616.4:p.Pro1301=
ENST00000220616.8:c.3903G>T	ENSP00000220616.4:p.Pro1301=
ENST00000523756.5:c.558G>T
NM_003235.4:c.3903G>T	NP_003226.4:p.Pro1301=
XM_005251038.3:c.3903G>T	XP_005251095.1:p.Pro1301=
XM_005251040.3:c.3903G>T	XP_005251097.1:p.Pro1301=
XM_005251042.3:c.3903G>T	XP_005251099.1:p.Pro1301=
XM_005251043.3:c.3903G>T	XP_005251100.1:p.Pro1301=
XM_006716622.2:c.3903G>T	XP_006716685.1:p.Pro1301=
XM_005251038.4:c.3903G>T	XP_005251095.1:p.Pro1301=
XM_005251040.4:c.3903G>T	XP_005251097.1:p.Pro1301=
XM_005251042.4:c.3903G>T	XP_005251099.1:p.Pro1301=
XM_006716622.3:c.3903G>T	XP_006716685.1:p.Pro1301=
XM_017013793.1:c.3903G>T	XP_016869282.1:p.Pro1301=
XM_017013794.1:c.3903G>T	XP_016869283.1:p.Pro1301=
XM_017013795.1:c.3903G>T	XP_016869284.1:p.Pro1301=
XM_017013796.1:c.3903G>T	XP_016869285.1:p.Pro1301=
XM_017013797.1:c.3642G>T	XP_016869286.1:p.Pro1214=
XM_017013798.1:c.3903G>T	XP_016869287.1:p.Pro1301=
XM_017013799.1:c.3903G>T	XP_016869288.1:p.Pro1301=
XM_017013800.1:c.3903G>T	XP_016869289.1:p.Pro1301=
NM_003235.5:c.3903G>T MANE Select	NP_003226.4:p.Pro1301=