Canonical Allele Identifier: CA372253409

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145823C>G (hg19) ; chr8:g.133133579C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133579C>G , CM000670.2:g.133133579C>G	GRCh38
NC_000008.10:g.134145823C>G , CM000670.1:g.134145823C>G	GRCh37
NC_000008.9:g.134215005C>G	NCBI36
NG_015832.1:g.271619C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8107C>G MANE Select	ENSP00000220616.4:p.Leu2703Val
ENST00000220616.8:c.8107C>G	ENSP00000220616.4:p.Leu2703Val
ENST00000519178.5:c.3473C>G
ENST00000519543.5:c.2506C>G	ENSP00000430430.1:p.Leu836Val
ENST00000521107.1:c.319C>G	ENSP00000430161.1:p.Leu107Val
ENST00000522691.1:n.193C>G
ENST00000523756.5:c.4762C>G
NM_003235.4:c.8107C>G	NP_003226.4:p.Leu2703Val
XM_005251038.3:c.7915C>G	XP_005251095.1:p.Leu2639Val
XM_006716622.2:c.8044C>G	XP_006716685.1:p.Leu2682Val
XM_005251038.4:c.7915C>G	XP_005251095.1:p.Leu2639Val
XM_006716622.3:c.8044C>G	XP_006716685.1:p.Leu2682Val
XM_017013793.1:c.8041C>G	XP_016869282.1:p.Leu2681Val
XM_017013794.1:c.7972C>G	XP_016869283.1:p.Leu2658Val
XM_017013795.1:c.7936C>G	XP_016869284.1:p.Leu2646Val
XM_017013796.1:c.7888C>G	XP_016869285.1:p.Leu2630Val
XM_017013797.1:c.7846C>G	XP_016869286.1:p.Leu2616Val
NM_003235.5:c.8107C>G MANE Select	NP_003226.4:p.Leu2703Val