Canonical Allele Identifier: CA372253584

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145869G>C (hg19) ; chr8:g.133133625G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133625G>C , CM000670.2:g.133133625G>C	GRCh38
NC_000008.10:g.134145869G>C , CM000670.1:g.134145869G>C	GRCh37
NC_000008.9:g.134215051G>C	NCBI36
NG_015832.1:g.271665G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8153G>C MANE Select	ENSP00000220616.4:p.Trp2718Ser
ENST00000220616.8:c.8153G>C	ENSP00000220616.4:p.Trp2718Ser
ENST00000519178.5:c.3519G>C
ENST00000519543.5:c.2552G>C	ENSP00000430430.1:p.Trp851Ser
ENST00000521107.1:c.365G>C	ENSP00000430161.1:p.Trp122Ser
ENST00000522691.1:n.239G>C
ENST00000523756.5:c.4808G>C
NM_003235.4:c.8153G>C	NP_003226.4:p.Trp2718Ser
XM_005251038.3:c.7961G>C	XP_005251095.1:p.Trp2654Ser
XM_006716622.2:c.8090G>C	XP_006716685.1:p.Trp2697Ser
XM_005251038.4:c.7961G>C	XP_005251095.1:p.Trp2654Ser
XM_006716622.3:c.8090G>C	XP_006716685.1:p.Trp2697Ser
XM_017013793.1:c.8087G>C	XP_016869282.1:p.Trp2696Ser
XM_017013794.1:c.8018G>C	XP_016869283.1:p.Trp2673Ser
XM_017013795.1:c.7982G>C	XP_016869284.1:p.Trp2661Ser
XM_017013796.1:c.7934G>C	XP_016869285.1:p.Trp2645Ser
XM_017013797.1:c.7892G>C	XP_016869286.1:p.Trp2631Ser
NM_003235.5:c.8153G>C MANE Select	NP_003226.4:p.Trp2718Ser