Canonical Allele Identifier: CA372253729

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145906T>A (hg19) ; chr8:g.133133662T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133662T>A , CM000670.2:g.133133662T>A	GRCh38
NC_000008.10:g.134145906T>A , CM000670.1:g.134145906T>A	GRCh37
NC_000008.9:g.134215088T>A	NCBI36
NG_015832.1:g.271702T>A

Transcript Alleles

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