Canonical Allele Identifier: CA372253433

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145830C>G (hg19) ; chr8:g.133133586C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133586C>G , CM000670.2:g.133133586C>G	GRCh38
NC_000008.10:g.134145830C>G , CM000670.1:g.134145830C>G	GRCh37
NC_000008.9:g.134215012C>G	NCBI36
NG_015832.1:g.271626C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8114C>G MANE Select	ENSP00000220616.4:p.Pro2705Arg
ENST00000220616.8:c.8114C>G	ENSP00000220616.4:p.Pro2705Arg
ENST00000519178.5:c.3480C>G
ENST00000519543.5:c.2513C>G	ENSP00000430430.1:p.Pro838Arg
ENST00000521107.1:c.326C>G	ENSP00000430161.1:p.Pro109Arg
ENST00000522691.1:n.200C>G
ENST00000523756.5:c.4769C>G
NM_003235.4:c.8114C>G	NP_003226.4:p.Pro2705Arg
XM_005251038.3:c.7922C>G	XP_005251095.1:p.Pro2641Arg
XM_006716622.2:c.8051C>G	XP_006716685.1:p.Pro2684Arg
XM_005251038.4:c.7922C>G	XP_005251095.1:p.Pro2641Arg
XM_006716622.3:c.8051C>G	XP_006716685.1:p.Pro2684Arg
XM_017013793.1:c.8048C>G	XP_016869282.1:p.Pro2683Arg
XM_017013794.1:c.7979C>G	XP_016869283.1:p.Pro2660Arg
XM_017013795.1:c.7943C>G	XP_016869284.1:p.Pro2648Arg
XM_017013796.1:c.7895C>G	XP_016869285.1:p.Pro2632Arg
XM_017013797.1:c.7853C>G	XP_016869286.1:p.Pro2618Arg
NM_003235.5:c.8114C>G MANE Select	NP_003226.4:p.Pro2705Arg