Canonical Allele Identifier: CA372253418

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145826C>G (hg19) ; chr8:g.133133582C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133582C>G , CM000670.2:g.133133582C>G	GRCh38
NC_000008.10:g.134145826C>G , CM000670.1:g.134145826C>G	GRCh37
NC_000008.9:g.134215008C>G	NCBI36
NG_015832.1:g.271622C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8110C>G MANE Select	ENSP00000220616.4:p.Leu2704Val
ENST00000220616.8:c.8110C>G	ENSP00000220616.4:p.Leu2704Val
ENST00000519178.5:c.3476C>G
ENST00000519543.5:c.2509C>G	ENSP00000430430.1:p.Leu837Val
ENST00000521107.1:c.322C>G	ENSP00000430161.1:p.Leu108Val
ENST00000522691.1:n.196C>G
ENST00000523756.5:c.4765C>G
NM_003235.4:c.8110C>G	NP_003226.4:p.Leu2704Val
XM_005251038.3:c.7918C>G	XP_005251095.1:p.Leu2640Val
XM_006716622.2:c.8047C>G	XP_006716685.1:p.Leu2683Val
XM_005251038.4:c.7918C>G	XP_005251095.1:p.Leu2640Val
XM_006716622.3:c.8047C>G	XP_006716685.1:p.Leu2683Val
XM_017013793.1:c.8044C>G	XP_016869282.1:p.Leu2682Val
XM_017013794.1:c.7975C>G	XP_016869283.1:p.Leu2659Val
XM_017013795.1:c.7939C>G	XP_016869284.1:p.Leu2647Val
XM_017013796.1:c.7891C>G	XP_016869285.1:p.Leu2631Val
XM_017013797.1:c.7849C>G	XP_016869286.1:p.Leu2617Val
NM_003235.5:c.8110C>G MANE Select	NP_003226.4:p.Leu2704Val