Canonical Allele Identifier: CA372253171

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145766C>T (hg19) ; chr8:g.133133522C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133522C>T , CM000670.2:g.133133522C>T	GRCh38
NC_000008.10:g.134145766C>T , CM000670.1:g.134145766C>T	GRCh37
NC_000008.9:g.134214948C>T	NCBI36
NG_015832.1:g.271562C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8050C>T MANE Select	ENSP00000220616.4:p.Pro2684Ser
ENST00000220616.8:c.8050C>T	ENSP00000220616.4:p.Pro2684Ser
ENST00000519178.5:c.3416C>T
ENST00000519543.5:c.2449C>T	ENSP00000430430.1:p.Pro817Ser
ENST00000521107.1:c.262C>T	ENSP00000430161.1:p.Pro88Ser
ENST00000522691.1:n.136C>T
ENST00000523756.5:c.4705C>T
NM_003235.4:c.8050C>T	NP_003226.4:p.Pro2684Ser
XM_005251038.3:c.7858C>T	XP_005251095.1:p.Pro2620Ser
XM_006716622.2:c.7987C>T	XP_006716685.1:p.Pro2663Ser
XM_005251038.4:c.7858C>T	XP_005251095.1:p.Pro2620Ser
XM_006716622.3:c.7987C>T	XP_006716685.1:p.Pro2663Ser
XM_017013793.1:c.7984C>T	XP_016869282.1:p.Pro2662Ser
XM_017013794.1:c.7915C>T	XP_016869283.1:p.Pro2639Ser
XM_017013795.1:c.7879C>T	XP_016869284.1:p.Pro2627Ser
XM_017013796.1:c.7831C>T	XP_016869285.1:p.Pro2611Ser
XM_017013797.1:c.7789C>T	XP_016869286.1:p.Pro2597Ser
NM_003235.5:c.8050C>T MANE Select	NP_003226.4:p.Pro2684Ser