Canonical Allele Identifier: CA372234874

Gene: TG

Linked Data

• ClinVar Variation Id: 2338559
• ClinVar RCV Id: RCV002936261
• dbSNP Id: rs1377074215
• gnomAD v4: 8-132888015-A-C
• MyVariant Identifiers: chr8:g.133900260A>C (hg19) ; chr8:g.132888015A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132888015A>C , CM000670.2:g.132888015A>C	GRCh38
NC_000008.10:g.133900260A>C , CM000670.1:g.133900260A>C	GRCh37
NC_000008.9:g.133969442A>C	NCBI36
NG_015832.1:g.26056A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000220616.9:c.2208A>C MANE Select	ENSP00000220616.4:p.Gln736His
ENST00000220616.8:c.2208A>C	ENSP00000220616.4:p.Gln736His
NM_003235.4:c.2208A>C	NP_003226.4:p.Gln736His
XM_005251038.3:c.2208A>C	XP_005251095.1:p.Gln736His
XM_005251040.3:c.2208A>C	XP_005251097.1:p.Gln736His
XM_005251042.3:c.2208A>C	XP_005251099.1:p.Gln736His
XM_005251043.3:c.2208A>C	XP_005251100.1:p.Gln736His
XM_006716622.2:c.2208A>C	XP_006716685.1:p.Gln736His
XM_005251038.4:c.2208A>C	XP_005251095.1:p.Gln736His
XM_005251040.4:c.2208A>C	XP_005251097.1:p.Gln736His
XM_005251042.4:c.2208A>C	XP_005251099.1:p.Gln736His
XM_006716622.3:c.2208A>C	XP_006716685.1:p.Gln736His
XM_017013793.1:c.2208A>C	XP_016869282.1:p.Gln736His
XM_017013794.1:c.2208A>C	XP_016869283.1:p.Gln736His
XM_017013795.1:c.2208A>C	XP_016869284.1:p.Gln736His
XM_017013796.1:c.2208A>C	XP_016869285.1:p.Gln736His
XM_017013797.1:c.1947A>C	XP_016869286.1:p.Gln649His
XM_017013798.1:c.2208A>C	XP_016869287.1:p.Gln736His
XM_017013799.1:c.2208A>C	XP_016869288.1:p.Gln736His
XM_017013800.1:c.2208A>C	XP_016869289.1:p.Gln736His
NM_003235.5:c.2208A>C MANE Select	NP_003226.4:p.Gln736His