Canonical Allele Identifier: CA1821005091

Gene: TG

Linked Data

• ClinVar Variation Id: 3044458
• ClinVar RCV Id: RCV004555701
• dbSNP Id: rs1829571049
• gnomAD v3: 8-132971879-A-G
• gnomAD v4: 8-132971879-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132971879A>G , CM000670.2:g.132971879A>G	GRCh38
NC_000008.10:g.133984124A>G , CM000670.1:g.133984124A>G	GRCh37
NC_000008.9:g.134053306A>G	NCBI36
NG_015832.1:g.109920A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6055+6A>G MANE Select	ENSP00000220616.4:n.6055+6A>G
ENST00000220616.8:c.6055+6A>G	ENSP00000220616.4:n.6055+6A>G
ENST00000519178.5:c.1421+6A>G
ENST00000519294.5:n.47+6A>G
ENST00000519543.5:c.517+6A>G	ENSP00000430430.1:n.517+6A>G
ENST00000520089.5:n.164+6A>G
ENST00000520197.5:n.192+6A>G
ENST00000523756.5:c.2710+6A>G
ENST00000524151.5:n.23+6A>G
NM_003235.4:c.6055+6A>G	NP_003226.4:n.6055+6A>G
XM_005251038.3:c.5863+6A>G	XP_005251095.1:n.5863+6A>G
XM_005251040.3:c.6055+6A>G	XP_005251097.1:n.6055+6A>G
XM_005251042.3:c.6055+6A>G	XP_005251099.1:n.6055+6A>G
XM_005251043.3:c.6055+6A>G	XP_005251100.1:n.6055+6A>G
XM_006716622.2:c.6055+6A>G	XP_006716685.1:n.6055+6A>G
XM_005251038.4:c.5863+6A>G	XP_005251095.1:n.5863+6A>G
XM_005251040.4:c.6055+6A>G	XP_005251097.1:n.6055+6A>G
XM_005251042.4:c.6055+6A>G	XP_005251099.1:n.6055+6A>G
XM_006716622.3:c.6055+6A>G	XP_006716685.1:n.6055+6A>G
XM_017013793.1:c.5989+6A>G	XP_016869282.1:n.5989+6A>G
XM_017013794.1:c.6055+6A>G	XP_016869283.1:n.6055+6A>G
XM_017013795.1:c.5884+6A>G	XP_016869284.1:n.5884+6A>G
XM_017013796.1:c.5836+6A>G	XP_016869285.1:n.5836+6A>G
XM_017013797.1:c.5794+6A>G	XP_016869286.1:n.5794+6A>G
XM_017013798.1:c.6055+6A>G	XP_016869287.1:n.6055+6A>G
XM_017013799.1:c.6055+6A>G	XP_016869288.1:n.6055+6A>G
XM_017013800.1:c.6055+6A>G	XP_016869289.1:n.6055+6A>G
NM_003235.5:c.6055+6A>G MANE Select	NP_003226.4:n.6055+6A>G