Canonical Allele Identifier: CA2688665275

Gene: TG

Linked Data

• dbSNP Id: rs2130425307
• gnomAD v4: 8-133133664-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133664G>A , CM000670.2:g.133133664G>A	GRCh38
NC_000008.10:g.134145908G>A , CM000670.1:g.134145908G>A	GRCh37
NC_000008.9:g.134215090G>A	NCBI36
NG_015832.1:g.271704G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8188+4G>A MANE Select	ENSP00000220616.4:n.8188+4G>A
ENST00000220616.8:c.8188+4G>A	ENSP00000220616.4:n.8188+4G>A
ENST00000519178.5:c.3554+4G>A
ENST00000519543.5:c.2587+4G>A	ENSP00000430430.1:n.2587+4G>A
ENST00000521107.1:c.400+4G>A	ENSP00000430161.1:n.400+4G>A
ENST00000522691.1:n.274+4G>A
ENST00000523756.5:c.4843+4G>A
NM_003235.4:c.8188+4G>A	NP_003226.4:n.8188+4G>A
XM_005251038.3:c.7996+4G>A	XP_005251095.1:n.7996+4G>A
XM_006716622.2:c.8125+4G>A	XP_006716685.1:n.8125+4G>A
XM_005251038.4:c.7996+4G>A	XP_005251095.1:n.7996+4G>A
XM_006716622.3:c.8125+4G>A	XP_006716685.1:n.8125+4G>A
XM_017013793.1:c.8122+4G>A	XP_016869282.1:n.8122+4G>A
XM_017013794.1:c.8053+4G>A	XP_016869283.1:n.8053+4G>A
XM_017013795.1:c.8017+4G>A	XP_016869284.1:n.8017+4G>A
XM_017013796.1:c.7969+4G>A	XP_016869285.1:n.7969+4G>A
XM_017013797.1:c.7927+4G>A	XP_016869286.1:n.7927+4G>A
NM_003235.5:c.8188+4G>A MANE Select	NP_003226.4:n.8188+4G>A