Canonical Allele Identifier: CA372253522

Gene: TG

Linked Data

• gnomAD v4: 8-133133608-A-T
• MyVariant Identifiers: chr8:g.134145852A>T (hg19) ; chr8:g.133133608A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133608A>T , CM000670.2:g.133133608A>T	GRCh38
NC_000008.10:g.134145852A>T , CM000670.1:g.134145852A>T	GRCh37
NC_000008.9:g.134215034A>T	NCBI36
NG_015832.1:g.271648A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8136A>T MANE Select	ENSP00000220616.4:p.Lys2712Asn
ENST00000220616.8:c.8136A>T	ENSP00000220616.4:p.Lys2712Asn
ENST00000519178.5:c.3502A>T
ENST00000519543.5:c.2535A>T	ENSP00000430430.1:p.Lys845Asn
ENST00000521107.1:c.348A>T	ENSP00000430161.1:p.Lys116Asn
ENST00000522691.1:n.222A>T
ENST00000523756.5:c.4791A>T
NM_003235.4:c.8136A>T	NP_003226.4:p.Lys2712Asn
XM_005251038.3:c.7944A>T	XP_005251095.1:p.Lys2648Asn
XM_006716622.2:c.8073A>T	XP_006716685.1:p.Lys2691Asn
XM_005251038.4:c.7944A>T	XP_005251095.1:p.Lys2648Asn
XM_006716622.3:c.8073A>T	XP_006716685.1:p.Lys2691Asn
XM_017013793.1:c.8070A>T	XP_016869282.1:p.Lys2690Asn
XM_017013794.1:c.8001A>T	XP_016869283.1:p.Lys2667Asn
XM_017013795.1:c.7965A>T	XP_016869284.1:p.Lys2655Asn
XM_017013796.1:c.7917A>T	XP_016869285.1:p.Lys2639Asn
XM_017013797.1:c.7875A>T	XP_016869286.1:p.Lys2625Asn
NM_003235.5:c.8136A>T MANE Select	NP_003226.4:p.Lys2712Asn