Canonical Allele Identifier: CA372253524

Gene: TG

Linked Data

• gnomAD v4: 8-133133609-G-T
• MyVariant Identifiers: chr8:g.134145853G>T (hg19) ; chr8:g.133133609G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133609G>T , CM000670.2:g.133133609G>T	GRCh38
NC_000008.10:g.134145853G>T , CM000670.1:g.134145853G>T	GRCh37
NC_000008.9:g.134215035G>T	NCBI36
NG_015832.1:g.271649G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8137G>T MANE Select	ENSP00000220616.4:p.Ala2713Ser
ENST00000220616.8:c.8137G>T	ENSP00000220616.4:p.Ala2713Ser
ENST00000519178.5:c.3503G>T
ENST00000519543.5:c.2536G>T	ENSP00000430430.1:p.Ala846Ser
ENST00000521107.1:c.349G>T	ENSP00000430161.1:p.Ala117Ser
ENST00000522691.1:n.223G>T
ENST00000523756.5:c.4792G>T
NM_003235.4:c.8137G>T	NP_003226.4:p.Ala2713Ser
XM_005251038.3:c.7945G>T	XP_005251095.1:p.Ala2649Ser
XM_006716622.2:c.8074G>T	XP_006716685.1:p.Ala2692Ser
XM_005251038.4:c.7945G>T	XP_005251095.1:p.Ala2649Ser
XM_006716622.3:c.8074G>T	XP_006716685.1:p.Ala2692Ser
XM_017013793.1:c.8071G>T	XP_016869282.1:p.Ala2691Ser
XM_017013794.1:c.8002G>T	XP_016869283.1:p.Ala2668Ser
XM_017013795.1:c.7966G>T	XP_016869284.1:p.Ala2656Ser
XM_017013796.1:c.7918G>T	XP_016869285.1:p.Ala2640Ser
XM_017013797.1:c.7876G>T	XP_016869286.1:p.Ala2626Ser
NM_003235.5:c.8137G>T MANE Select	NP_003226.4:p.Ala2713Ser