Canonical Allele Identifier: CA372253222

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145778T>C (hg19) ; chr8:g.133133534T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133534T>C , CM000670.2:g.133133534T>C	GRCh38
NC_000008.10:g.134145778T>C , CM000670.1:g.134145778T>C	GRCh37
NC_000008.9:g.134214960T>C	NCBI36
NG_015832.1:g.271574T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8062T>C MANE Select	ENSP00000220616.4:p.Phe2688Leu
ENST00000220616.8:c.8062T>C	ENSP00000220616.4:p.Phe2688Leu
ENST00000519178.5:c.3428T>C
ENST00000519543.5:c.2461T>C	ENSP00000430430.1:p.Phe821Leu
ENST00000521107.1:c.274T>C	ENSP00000430161.1:p.Phe92Leu
ENST00000522691.1:n.148T>C
ENST00000523756.5:c.4717T>C
NM_003235.4:c.8062T>C	NP_003226.4:p.Phe2688Leu
XM_005251038.3:c.7870T>C	XP_005251095.1:p.Phe2624Leu
XM_006716622.2:c.7999T>C	XP_006716685.1:p.Phe2667Leu
XM_005251038.4:c.7870T>C	XP_005251095.1:p.Phe2624Leu
XM_006716622.3:c.7999T>C	XP_006716685.1:p.Phe2667Leu
XM_017013793.1:c.7996T>C	XP_016869282.1:p.Phe2666Leu
XM_017013794.1:c.7927T>C	XP_016869283.1:p.Phe2643Leu
XM_017013795.1:c.7891T>C	XP_016869284.1:p.Phe2631Leu
XM_017013796.1:c.7843T>C	XP_016869285.1:p.Phe2615Leu
XM_017013797.1:c.7801T>C	XP_016869286.1:p.Phe2601Leu
NM_003235.5:c.8062T>C MANE Select	NP_003226.4:p.Phe2688Leu