Canonical Allele Identifier: CA372233916

Gene: TG

Linked Data

• dbSNP Id: rs1835196793
• MyVariant Identifiers: chr8:g.134030234C>G (hg19) ; chr8:g.133017989C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133017989C>G , CM000670.2:g.133017989C>G	GRCh38
NC_000008.10:g.134030234C>G , CM000670.1:g.134030234C>G	GRCh37
NC_000008.9:g.134099416C>G	NCBI36
NG_015832.1:g.156030C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6774C>G MANE Select	ENSP00000220616.4:p.Ser2258Arg
ENST00000220616.8:c.6774C>G	ENSP00000220616.4:p.Ser2258Arg
ENST00000518108.1:c.168+123C>G
ENST00000519178.5:c.2140C>G
ENST00000519543.5:c.1173C>G	ENSP00000430430.1:p.Ser391Arg
ENST00000523756.5:c.3429C>G
NM_003235.4:c.6774C>G	NP_003226.4:p.Ser2258Arg
XM_005251038.3:c.6582C>G	XP_005251095.1:p.Ser2194Arg
XM_006716622.2:c.6711C>G	XP_006716685.1:p.Ser2237Arg
XM_005251038.4:c.6582C>G	XP_005251095.1:p.Ser2194Arg
XM_006716622.3:c.6711C>G	XP_006716685.1:p.Ser2237Arg
XM_017013793.1:c.6708C>G	XP_016869282.1:p.Ser2236Arg
XM_017013794.1:c.6774C>G	XP_016869283.1:p.Ser2258Arg
XM_017013795.1:c.6603C>G	XP_016869284.1:p.Ser2201Arg
XM_017013796.1:c.6555C>G	XP_016869285.1:p.Ser2185Arg
XM_017013797.1:c.6513C>G	XP_016869286.1:p.Ser2171Arg
XM_017013798.1:c.6774C>G	XP_016869287.1:p.Ser2258Arg
NM_003235.5:c.6774C>G MANE Select	NP_003226.4:p.Ser2258Arg