Canonical Allele Identifier: CA372253573

Gene: TG

Linked Data

• gnomAD v4: 8-133133623-C-G
• MyVariant Identifiers: chr8:g.134145867C>G (hg19) ; chr8:g.133133623C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133623C>G , CM000670.2:g.133133623C>G	GRCh38
NC_000008.10:g.134145867C>G , CM000670.1:g.134145867C>G	GRCh37
NC_000008.9:g.134215049C>G	NCBI36
NG_015832.1:g.271663C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8151C>G MANE Select	ENSP00000220616.4:p.Phe2717Leu
ENST00000220616.8:c.8151C>G	ENSP00000220616.4:p.Phe2717Leu
ENST00000519178.5:c.3517C>G
ENST00000519543.5:c.2550C>G	ENSP00000430430.1:p.Phe850Leu
ENST00000521107.1:c.363C>G	ENSP00000430161.1:p.Phe121Leu
ENST00000522691.1:n.237C>G
ENST00000523756.5:c.4806C>G
NM_003235.4:c.8151C>G	NP_003226.4:p.Phe2717Leu
XM_005251038.3:c.7959C>G	XP_005251095.1:p.Phe2653Leu
XM_006716622.2:c.8088C>G	XP_006716685.1:p.Phe2696Leu
XM_005251038.4:c.7959C>G	XP_005251095.1:p.Phe2653Leu
XM_006716622.3:c.8088C>G	XP_006716685.1:p.Phe2696Leu
XM_017013793.1:c.8085C>G	XP_016869282.1:p.Phe2695Leu
XM_017013794.1:c.8016C>G	XP_016869283.1:p.Phe2672Leu
XM_017013795.1:c.7980C>G	XP_016869284.1:p.Phe2660Leu
XM_017013796.1:c.7932C>G	XP_016869285.1:p.Phe2644Leu
XM_017013797.1:c.7890C>G	XP_016869286.1:p.Phe2630Leu
NM_003235.5:c.8151C>G MANE Select	NP_003226.4:p.Phe2717Leu