Canonical Allele Identifier: CA372253261

Gene: TG

Linked Data

• dbSNP Id: rs531167775
• gnomAD v2: 8-134145788-G-C
• gnomAD v4: 8-133133544-G-C
• MyVariant Identifiers: chr8:g.134145788G>C (hg19) ; chr8:g.133133544G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133544G>C , CM000670.2:g.133133544G>C	GRCh38
NC_000008.10:g.134145788G>C , CM000670.1:g.134145788G>C	GRCh37
NC_000008.9:g.134214970G>C	NCBI36
NG_015832.1:g.271584G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8072G>C MANE Select	ENSP00000220616.4:p.Arg2691Pro
ENST00000220616.8:c.8072G>C	ENSP00000220616.4:p.Arg2691Pro
ENST00000519178.5:c.3438G>C
ENST00000519543.5:c.2471G>C	ENSP00000430430.1:p.Arg824Pro
ENST00000521107.1:c.284G>C	ENSP00000430161.1:p.Arg95Pro
ENST00000522691.1:n.158G>C
ENST00000523756.5:c.4727G>C
NM_003235.4:c.8072G>C	NP_003226.4:p.Arg2691Pro
XM_005251038.3:c.7880G>C	XP_005251095.1:p.Arg2627Pro
XM_006716622.2:c.8009G>C	XP_006716685.1:p.Arg2670Pro
XM_005251038.4:c.7880G>C	XP_005251095.1:p.Arg2627Pro
XM_006716622.3:c.8009G>C	XP_006716685.1:p.Arg2670Pro
XM_017013793.1:c.8006G>C	XP_016869282.1:p.Arg2669Pro
XM_017013794.1:c.7937G>C	XP_016869283.1:p.Arg2646Pro
XM_017013795.1:c.7901G>C	XP_016869284.1:p.Arg2634Pro
XM_017013796.1:c.7853G>C	XP_016869285.1:p.Arg2618Pro
XM_017013797.1:c.7811G>C	XP_016869286.1:p.Arg2604Pro
NM_003235.5:c.8072G>C MANE Select	NP_003226.4:p.Arg2691Pro