Canonical Allele Identifier: CA372253420

Gene: TG

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8110C>T MANE Select	ENSP00000220616.4:p.Leu2704Phe
ENST00000220616.8:c.8110C>T	ENSP00000220616.4:p.Leu2704Phe
ENST00000519178.5:c.3476C>T
ENST00000519543.5:c.2509C>T	ENSP00000430430.1:p.Leu837Phe
ENST00000521107.1:c.322C>T	ENSP00000430161.1:p.Leu108Phe
ENST00000522691.1:n.196C>T
ENST00000523756.5:c.4765C>T
NM_003235.4:c.8110C>T	NP_003226.4:p.Leu2704Phe
XM_005251038.3:c.7918C>T	XP_005251095.1:p.Leu2640Phe
XM_006716622.2:c.8047C>T	XP_006716685.1:p.Leu2683Phe
XM_005251038.4:c.7918C>T	XP_005251095.1:p.Leu2640Phe
XM_006716622.3:c.8047C>T	XP_006716685.1:p.Leu2683Phe
XM_017013793.1:c.8044C>T	XP_016869282.1:p.Leu2682Phe
XM_017013794.1:c.7975C>T	XP_016869283.1:p.Leu2659Phe
XM_017013795.1:c.7939C>T	XP_016869284.1:p.Leu2647Phe
XM_017013796.1:c.7891C>T	XP_016869285.1:p.Leu2631Phe
XM_017013797.1:c.7849C>T	XP_016869286.1:p.Leu2617Phe
NM_003235.5:c.8110C>T MANE Select	NP_003226.4:p.Leu2704Phe