Canonical Allele Identifier: CA372253634

Gene: TG

Linked Data

• gnomAD v4: 8-133133634-A-T
• MyVariant Identifiers: chr8:g.134145878A>T (hg19) ; chr8:g.133133634A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133634A>T , CM000670.2:g.133133634A>T	GRCh38
NC_000008.10:g.134145878A>T , CM000670.1:g.134145878A>T	GRCh37
NC_000008.9:g.134215060A>T	NCBI36
NG_015832.1:g.271674A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8162A>T MANE Select	ENSP00000220616.4:p.Tyr2721Phe
ENST00000220616.8:c.8162A>T	ENSP00000220616.4:p.Tyr2721Phe
ENST00000519178.5:c.3528A>T
ENST00000519543.5:c.2561A>T	ENSP00000430430.1:p.Tyr854Phe
ENST00000521107.1:c.374A>T	ENSP00000430161.1:p.Tyr125Phe
ENST00000522691.1:n.248A>T
ENST00000523756.5:c.4817A>T
NM_003235.4:c.8162A>T	NP_003226.4:p.Tyr2721Phe
XM_005251038.3:c.7970A>T	XP_005251095.1:p.Tyr2657Phe
XM_006716622.2:c.8099A>T	XP_006716685.1:p.Tyr2700Phe
XM_005251038.4:c.7970A>T	XP_005251095.1:p.Tyr2657Phe
XM_006716622.3:c.8099A>T	XP_006716685.1:p.Tyr2700Phe
XM_017013793.1:c.8096A>T	XP_016869282.1:p.Tyr2699Phe
XM_017013794.1:c.8027A>T	XP_016869283.1:p.Tyr2676Phe
XM_017013795.1:c.7991A>T	XP_016869284.1:p.Tyr2664Phe
XM_017013796.1:c.7943A>T	XP_016869285.1:p.Tyr2648Phe
XM_017013797.1:c.7901A>T	XP_016869286.1:p.Tyr2634Phe
NM_003235.5:c.8162A>T MANE Select	NP_003226.4:p.Tyr2721Phe