Canonical Allele Identifier: CA372253674

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145889C>G (hg19) ; chr8:g.133133645C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133645C>G , CM000670.2:g.133133645C>G	GRCh38
NC_000008.10:g.134145889C>G , CM000670.1:g.134145889C>G	GRCh37
NC_000008.9:g.134215071C>G	NCBI36
NG_015832.1:g.271685C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8173C>G MANE Select	ENSP00000220616.4:p.Leu2725Val
ENST00000220616.8:c.8173C>G	ENSP00000220616.4:p.Leu2725Val
ENST00000519178.5:c.3539C>G
ENST00000519543.5:c.2572C>G	ENSP00000430430.1:p.Leu858Val
ENST00000521107.1:c.385C>G	ENSP00000430161.1:p.Leu129Val
ENST00000522691.1:n.259C>G
ENST00000523756.5:c.4828C>G
NM_003235.4:c.8173C>G	NP_003226.4:p.Leu2725Val
XM_005251038.3:c.7981C>G	XP_005251095.1:p.Leu2661Val
XM_006716622.2:c.8110C>G	XP_006716685.1:p.Leu2704Val
XM_005251038.4:c.7981C>G	XP_005251095.1:p.Leu2661Val
XM_006716622.3:c.8110C>G	XP_006716685.1:p.Leu2704Val
XM_017013793.1:c.8107C>G	XP_016869282.1:p.Leu2703Val
XM_017013794.1:c.8038C>G	XP_016869283.1:p.Leu2680Val
XM_017013795.1:c.8002C>G	XP_016869284.1:p.Leu2668Val
XM_017013796.1:c.7954C>G	XP_016869285.1:p.Leu2652Val
XM_017013797.1:c.7912C>G	XP_016869286.1:p.Leu2638Val
NM_003235.5:c.8173C>G MANE Select	NP_003226.4:p.Leu2725Val