Canonical Allele Identifier: CA372253104

Gene: TG

Linked Data

• dbSNP Id: rs1852103735
• gnomAD v3: 8-133133504-G-C
• gnomAD v4: 8-133133504-G-C
• MyVariant Identifiers: chr8:g.134145748G>C (hg19) ; chr8:g.133133504G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133504G>C , CM000670.2:g.133133504G>C	GRCh38
NC_000008.10:g.134145748G>C , CM000670.1:g.134145748G>C	GRCh37
NC_000008.9:g.134214930G>C	NCBI36
NG_015832.1:g.271544G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8032G>C MANE Select	ENSP00000220616.4:p.Val2678Leu
ENST00000220616.8:c.8032G>C	ENSP00000220616.4:p.Val2678Leu
ENST00000519178.5:c.3398G>C
ENST00000519543.5:c.2431G>C	ENSP00000430430.1:p.Val811Leu
ENST00000521107.1:c.244G>C	ENSP00000430161.1:p.Val82Leu
ENST00000522691.1:n.118G>C
ENST00000523756.5:c.4687G>C
NM_003235.4:c.8032G>C	NP_003226.4:p.Val2678Leu
XM_005251038.3:c.7840G>C	XP_005251095.1:p.Val2614Leu
XM_006716622.2:c.7969G>C	XP_006716685.1:p.Val2657Leu
XM_005251038.4:c.7840G>C	XP_005251095.1:p.Val2614Leu
XM_006716622.3:c.7969G>C	XP_006716685.1:p.Val2657Leu
XM_017013793.1:c.7966G>C	XP_016869282.1:p.Val2656Leu
XM_017013794.1:c.7897G>C	XP_016869283.1:p.Val2633Leu
XM_017013795.1:c.7861G>C	XP_016869284.1:p.Val2621Leu
XM_017013796.1:c.7813G>C	XP_016869285.1:p.Val2605Leu
XM_017013797.1:c.7771G>C	XP_016869286.1:p.Val2591Leu
NM_003235.5:c.8032G>C MANE Select	NP_003226.4:p.Val2678Leu