Canonical Allele Identifier: CA372253567

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145865T>C (hg19) ; chr8:g.133133621T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133621T>C , CM000670.2:g.133133621T>C	GRCh38
NC_000008.10:g.134145865T>C , CM000670.1:g.134145865T>C	GRCh37
NC_000008.9:g.134215047T>C	NCBI36
NG_015832.1:g.271661T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8149T>C MANE Select	ENSP00000220616.4:p.Phe2717Leu
ENST00000220616.8:c.8149T>C	ENSP00000220616.4:p.Phe2717Leu
ENST00000519178.5:c.3515T>C
ENST00000519543.5:c.2548T>C	ENSP00000430430.1:p.Phe850Leu
ENST00000521107.1:c.361T>C	ENSP00000430161.1:p.Phe121Leu
ENST00000522691.1:n.235T>C
ENST00000523756.5:c.4804T>C
NM_003235.4:c.8149T>C	NP_003226.4:p.Phe2717Leu
XM_005251038.3:c.7957T>C	XP_005251095.1:p.Phe2653Leu
XM_006716622.2:c.8086T>C	XP_006716685.1:p.Phe2696Leu
XM_005251038.4:c.7957T>C	XP_005251095.1:p.Phe2653Leu
XM_006716622.3:c.8086T>C	XP_006716685.1:p.Phe2696Leu
XM_017013793.1:c.8083T>C	XP_016869282.1:p.Phe2695Leu
XM_017013794.1:c.8014T>C	XP_016869283.1:p.Phe2672Leu
XM_017013795.1:c.7978T>C	XP_016869284.1:p.Phe2660Leu
XM_017013796.1:c.7930T>C	XP_016869285.1:p.Phe2644Leu
XM_017013797.1:c.7888T>C	XP_016869286.1:p.Phe2630Leu
NM_003235.5:c.8149T>C MANE Select	NP_003226.4:p.Phe2717Leu