Canonical Allele Identifier: CA463017012

Gene: TG

Linked Data

• gnomAD v4: 8-133133497-A-C
• MyVariant Identifiers: chr8:g.134145741A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133497A>C , CM000670.2:g.133133497A>C	GRCh38
NC_000008.10:g.134145741A>C , CM000670.1:g.134145741A>C	GRCh37
NC_000008.9:g.134214923A>C	NCBI36
NG_015832.1:g.271537A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8025A>C MANE Select	ENSP00000220616.4:p.Ser2675=
ENST00000220616.8:c.8025A>C	ENSP00000220616.4:p.Ser2675=
ENST00000519178.5:c.3391A>C
ENST00000519543.5:c.2424A>C	ENSP00000430430.1:p.Ser808=
ENST00000521107.1:c.237A>C	ENSP00000430161.1:p.Ser79=
ENST00000522691.1:n.111A>C
ENST00000523756.5:c.4680A>C
NM_003235.4:c.8025A>C	NP_003226.4:p.Ser2675=
XM_005251038.3:c.7833A>C	XP_005251095.1:p.Ser2611=
XM_006716622.2:c.7962A>C	XP_006716685.1:p.Ser2654=
XM_005251038.4:c.7833A>C	XP_005251095.1:p.Ser2611=
XM_006716622.3:c.7962A>C	XP_006716685.1:p.Ser2654=
XM_017013793.1:c.7959A>C	XP_016869282.1:p.Ser2653=
XM_017013794.1:c.7890A>C	XP_016869283.1:p.Ser2630=
XM_017013795.1:c.7854A>C	XP_016869284.1:p.Ser2618=
XM_017013796.1:c.7806A>C	XP_016869285.1:p.Ser2602=
XM_017013797.1:c.7764A>C	XP_016869286.1:p.Ser2588=
NM_003235.5:c.8025A>C MANE Select	NP_003226.4:p.Ser2675=