Canonical Allele Identifier: CA372253196

Gene: TG

Linked Data

• dbSNP Id: rs1852105876
• MyVariant Identifiers: chr8:g.134145772C>G (hg19) ; chr8:g.133133528C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133528C>G , CM000670.2:g.133133528C>G	GRCh38
NC_000008.10:g.134145772C>G , CM000670.1:g.134145772C>G	GRCh37
NC_000008.9:g.134214954C>G	NCBI36
NG_015832.1:g.271568C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8056C>G MANE Select	ENSP00000220616.4:p.Pro2686Ala
ENST00000220616.8:c.8056C>G	ENSP00000220616.4:p.Pro2686Ala
ENST00000519178.5:c.3422C>G
ENST00000519543.5:c.2455C>G	ENSP00000430430.1:p.Pro819Ala
ENST00000521107.1:c.268C>G	ENSP00000430161.1:p.Pro90Ala
ENST00000522691.1:n.142C>G
ENST00000523756.5:c.4711C>G
NM_003235.4:c.8056C>G	NP_003226.4:p.Pro2686Ala
XM_005251038.3:c.7864C>G	XP_005251095.1:p.Pro2622Ala
XM_006716622.2:c.7993C>G	XP_006716685.1:p.Pro2665Ala
XM_005251038.4:c.7864C>G	XP_005251095.1:p.Pro2622Ala
XM_006716622.3:c.7993C>G	XP_006716685.1:p.Pro2665Ala
XM_017013793.1:c.7990C>G	XP_016869282.1:p.Pro2664Ala
XM_017013794.1:c.7921C>G	XP_016869283.1:p.Pro2641Ala
XM_017013795.1:c.7885C>G	XP_016869284.1:p.Pro2629Ala
XM_017013796.1:c.7837C>G	XP_016869285.1:p.Pro2613Ala
XM_017013797.1:c.7795C>G	XP_016869286.1:p.Pro2599Ala
NM_003235.5:c.8056C>G MANE Select	NP_003226.4:p.Pro2686Ala