Canonical Allele Identifier: CA463016995

Gene: TG

Linked Data

• gnomAD v4: 8-133133485-T-G
• MyVariant Identifiers: chr8:g.134145729T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133485T>G , CM000670.2:g.133133485T>G	GRCh38
NC_000008.10:g.134145729T>G , CM000670.1:g.134145729T>G	GRCh37
NC_000008.9:g.134214911T>G	NCBI36
NG_015832.1:g.271525T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8013T>G MANE Select	ENSP00000220616.4:p.Pro2671=
ENST00000220616.8:c.8013T>G	ENSP00000220616.4:p.Pro2671=
ENST00000519178.5:c.3379T>G
ENST00000519543.5:c.2412T>G	ENSP00000430430.1:p.Pro804=
ENST00000521107.1:c.225T>G	ENSP00000430161.1:p.Pro75=
ENST00000522691.1:n.99T>G
ENST00000523756.5:c.4668T>G
NM_003235.4:c.8013T>G	NP_003226.4:p.Pro2671=
XM_005251038.3:c.7821T>G	XP_005251095.1:p.Pro2607=
XM_006716622.2:c.7950T>G	XP_006716685.1:p.Pro2650=
XM_005251038.4:c.7821T>G	XP_005251095.1:p.Pro2607=
XM_006716622.3:c.7950T>G	XP_006716685.1:p.Pro2650=
XM_017013793.1:c.7947T>G	XP_016869282.1:p.Pro2649=
XM_017013794.1:c.7878T>G	XP_016869283.1:p.Pro2626=
XM_017013795.1:c.7842T>G	XP_016869284.1:p.Pro2614=
XM_017013796.1:c.7794T>G	XP_016869285.1:p.Pro2598=
XM_017013797.1:c.7752T>G	XP_016869286.1:p.Pro2584=
NM_003235.5:c.8013T>G MANE Select	NP_003226.4:p.Pro2671=