Canonical Allele Identifier: CA186356886

Gene: TG

Linked Data

• dbSNP Id: rs900697094
• gnomAD v4: 8-133133622-T-C
• MyVariant Identifiers: chr8:g.134145866T>C (hg19) ; chr8:g.133133622T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133622T>C , CM000670.2:g.133133622T>C	GRCh38
NC_000008.10:g.134145866T>C , CM000670.1:g.134145866T>C	GRCh37
NC_000008.9:g.134215048T>C	NCBI36
NG_015832.1:g.271662T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8150T>C MANE Select	ENSP00000220616.4:p.Phe2717Ser
ENST00000220616.8:c.8150T>C	ENSP00000220616.4:p.Phe2717Ser
ENST00000519178.5:c.3516T>C
ENST00000519543.5:c.2549T>C	ENSP00000430430.1:p.Phe850Ser
ENST00000521107.1:c.362T>C	ENSP00000430161.1:p.Phe121Ser
ENST00000522691.1:n.236T>C
ENST00000523756.5:c.4805T>C
NM_003235.4:c.8150T>C	NP_003226.4:p.Phe2717Ser
XM_005251038.3:c.7958T>C	XP_005251095.1:p.Phe2653Ser
XM_006716622.2:c.8087T>C	XP_006716685.1:p.Phe2696Ser
XM_005251038.4:c.7958T>C	XP_005251095.1:p.Phe2653Ser
XM_006716622.3:c.8087T>C	XP_006716685.1:p.Phe2696Ser
XM_017013793.1:c.8084T>C	XP_016869282.1:p.Phe2695Ser
XM_017013794.1:c.8015T>C	XP_016869283.1:p.Phe2672Ser
XM_017013795.1:c.7979T>C	XP_016869284.1:p.Phe2660Ser
XM_017013796.1:c.7931T>C	XP_016869285.1:p.Phe2644Ser
XM_017013797.1:c.7889T>C	XP_016869286.1:p.Phe2630Ser
NM_003235.5:c.8150T>C MANE Select	NP_003226.4:p.Phe2717Ser