Canonical Allele Identifier: CA463012850

Gene: TG

Linked Data

• ClinVar Variation Id: 2876165
• ClinVar RCV Id: RCV003710091
• dbSNP Id: rs1401112031
• gnomAD v2: 8-133984060-G-C
• gnomAD v4: 8-132971815-G-C
• MyVariant Identifiers: chr8:g.133984060G>C (hg19) ; chr8:g.132971815G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132971815G>C , CM000670.2:g.132971815G>C	GRCh38
NC_000008.10:g.133984060G>C , CM000670.1:g.133984060G>C	GRCh37
NC_000008.9:g.134053242G>C	NCBI36
NG_015832.1:g.109856G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.5997G>C MANE Select	ENSP00000220616.4:p.Arg1999=
ENST00000220616.8:c.5997G>C	ENSP00000220616.4:p.Arg1999=
ENST00000519178.5:c.1363G>C
ENST00000519543.5:c.459G>C	ENSP00000430430.1:p.Arg153=
ENST00000520089.5:n.106G>C
ENST00000520197.5:n.134G>C
ENST00000523756.5:c.2652G>C
NM_003235.4:c.5997G>C	NP_003226.4:p.Arg1999=
XM_005251038.3:c.5805G>C	XP_005251095.1:p.Arg1935=
XM_005251040.3:c.5997G>C	XP_005251097.1:p.Arg1999=
XM_005251042.3:c.5997G>C	XP_005251099.1:p.Arg1999=
XM_005251043.3:c.5997G>C	XP_005251100.1:p.Arg1999=
XM_006716622.2:c.5997G>C	XP_006716685.1:p.Arg1999=
XM_005251038.4:c.5805G>C	XP_005251095.1:p.Arg1935=
XM_005251040.4:c.5997G>C	XP_005251097.1:p.Arg1999=
XM_005251042.4:c.5997G>C	XP_005251099.1:p.Arg1999=
XM_006716622.3:c.5997G>C	XP_006716685.1:p.Arg1999=
XM_017013793.1:c.5931G>C	XP_016869282.1:p.Arg1977=
XM_017013794.1:c.5997G>C	XP_016869283.1:p.Arg1999=
XM_017013795.1:c.5826G>C	XP_016869284.1:p.Arg1942=
XM_017013796.1:c.5778G>C	XP_016869285.1:p.Arg1926=
XM_017013797.1:c.5736G>C	XP_016869286.1:p.Arg1912=
XM_017013798.1:c.5997G>C	XP_016869287.1:p.Arg1999=
XM_017013799.1:c.5997G>C	XP_016869288.1:p.Arg1999=
XM_017013800.1:c.5997G>C	XP_016869289.1:p.Arg1999=
NM_003235.5:c.5997G>C MANE Select	NP_003226.4:p.Arg1999=