Canonical Allele Identifier: CA372253552

Gene: TG

Linked Data

• gnomAD v4: 8-133133617-C-G
• MyVariant Identifiers: chr8:g.134145861C>G (hg19) ; chr8:g.133133617C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133617C>G , CM000670.2:g.133133617C>G	GRCh38
NC_000008.10:g.134145861C>G , CM000670.1:g.134145861C>G	GRCh37
NC_000008.9:g.134215043C>G	NCBI36
NG_015832.1:g.271657C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8145C>G MANE Select	ENSP00000220616.4:p.Cys2715Trp
ENST00000220616.8:c.8145C>G	ENSP00000220616.4:p.Cys2715Trp
ENST00000519178.5:c.3511C>G
ENST00000519543.5:c.2544C>G	ENSP00000430430.1:p.Cys848Trp
ENST00000521107.1:c.357C>G	ENSP00000430161.1:p.Cys119Trp
ENST00000522691.1:n.231C>G
ENST00000523756.5:c.4800C>G
NM_003235.4:c.8145C>G	NP_003226.4:p.Cys2715Trp
XM_005251038.3:c.7953C>G	XP_005251095.1:p.Cys2651Trp
XM_006716622.2:c.8082C>G	XP_006716685.1:p.Cys2694Trp
XM_005251038.4:c.7953C>G	XP_005251095.1:p.Cys2651Trp
XM_006716622.3:c.8082C>G	XP_006716685.1:p.Cys2694Trp
XM_017013793.1:c.8079C>G	XP_016869282.1:p.Cys2693Trp
XM_017013794.1:c.8010C>G	XP_016869283.1:p.Cys2670Trp
XM_017013795.1:c.7974C>G	XP_016869284.1:p.Cys2658Trp
XM_017013796.1:c.7926C>G	XP_016869285.1:p.Cys2642Trp
XM_017013797.1:c.7884C>G	XP_016869286.1:p.Cys2628Trp
NM_003235.5:c.8145C>G MANE Select	NP_003226.4:p.Cys2715Trp