Canonical Allele Identifier: CA2688649314

Gene: TG

Linked Data

• gnomAD v4: 8-132897624-T-TGCTTTTCTCCTTCCCTGACTCCAGCCTTAA

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132897629_132897658dup , CM000670.2:g.132897629_132897658dup	GRCh38
NC_000008.10:g.133909874_133909903dup , CM000670.1:g.133909874_133909903dup	GRCh37
NC_000008.9:g.133979056_133979085dup	NCBI36
NG_015832.1:g.35670_35699dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000220616.9:c.3002-20_3011dup
ENST00000220616.8:c.3002-20_3011dup
NM_003235.4:c.3002-20_3011dup
XM_005251038.3:c.3002-20_3011dup
XM_005251040.3:c.3002-20_3011dup
XM_005251042.3:c.3002-20_3011dup
XM_005251043.3:c.3002-20_3011dup
XM_006716622.2:c.3002-20_3011dup
XM_005251038.4:c.3002-20_3011dup
XM_005251040.4:c.3002-20_3011dup
XM_005251042.4:c.3002-20_3011dup
XM_006716622.3:c.3002-20_3011dup
XM_017013793.1:c.3002-20_3011dup
XM_017013794.1:c.3002-20_3011dup
XM_017013795.1:c.3002-20_3011dup
XM_017013796.1:c.3002-20_3011dup
XM_017013797.1:c.2741-20_2750dup
XM_017013798.1:c.3002-20_3011dup
XM_017013799.1:c.3002-20_3011dup
XM_017013800.1:c.3002-20_3011dup
NM_003235.5:c.3002-20_3011dup