Canonical Allele Identifier: CA372253016

Gene: TG

Linked Data

• dbSNP Id: rs757851867
• gnomAD v3: 8-133133483-C-A
• gnomAD v4: 8-133133483-C-A
• MyVariant Identifiers: chr8:g.134145727C>A (hg19) ; chr8:g.133133483C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133483C>A , CM000670.2:g.133133483C>A	GRCh38
NC_000008.10:g.134145727C>A , CM000670.1:g.134145727C>A	GRCh37
NC_000008.9:g.134214909C>A	NCBI36
NG_015832.1:g.271523C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8011C>A MANE Select	ENSP00000220616.4:p.Pro2671Thr
ENST00000220616.8:c.8011C>A	ENSP00000220616.4:p.Pro2671Thr
ENST00000519178.5:c.3377C>A
ENST00000519543.5:c.2410C>A	ENSP00000430430.1:p.Pro804Thr
ENST00000521107.1:c.223C>A	ENSP00000430161.1:p.Pro75Thr
ENST00000522691.1:n.97C>A
ENST00000523756.5:c.4666C>A
NM_003235.4:c.8011C>A	NP_003226.4:p.Pro2671Thr
XM_005251038.3:c.7819C>A	XP_005251095.1:p.Pro2607Thr
XM_006716622.2:c.7948C>A	XP_006716685.1:p.Pro2650Thr
XM_005251038.4:c.7819C>A	XP_005251095.1:p.Pro2607Thr
XM_006716622.3:c.7948C>A	XP_006716685.1:p.Pro2650Thr
XM_017013793.1:c.7945C>A	XP_016869282.1:p.Pro2649Thr
XM_017013794.1:c.7876C>A	XP_016869283.1:p.Pro2626Thr
XM_017013795.1:c.7840C>A	XP_016869284.1:p.Pro2614Thr
XM_017013796.1:c.7792C>A	XP_016869285.1:p.Pro2598Thr
XM_017013797.1:c.7750C>A	XP_016869286.1:p.Pro2584Thr
NM_003235.5:c.8011C>A MANE Select	NP_003226.4:p.Pro2671Thr