Canonical Allele Identifier: CA372233910

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134030232A>C (hg19) ; chr8:g.133017987A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133017987A>C , CM000670.2:g.133017987A>C	GRCh38
NC_000008.10:g.134030232A>C , CM000670.1:g.134030232A>C	GRCh37
NC_000008.9:g.134099414A>C	NCBI36
NG_015832.1:g.156028A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6772A>C MANE Select	ENSP00000220616.4:p.Ser2258Arg
ENST00000220616.8:c.6772A>C	ENSP00000220616.4:p.Ser2258Arg
ENST00000518108.1:c.168+121A>C
ENST00000519178.5:c.2138A>C
ENST00000519543.5:c.1171A>C	ENSP00000430430.1:p.Ser391Arg
ENST00000523756.5:c.3427A>C
NM_003235.4:c.6772A>C	NP_003226.4:p.Ser2258Arg
XM_005251038.3:c.6580A>C	XP_005251095.1:p.Ser2194Arg
XM_006716622.2:c.6709A>C	XP_006716685.1:p.Ser2237Arg
XM_005251038.4:c.6580A>C	XP_005251095.1:p.Ser2194Arg
XM_006716622.3:c.6709A>C	XP_006716685.1:p.Ser2237Arg
XM_017013793.1:c.6706A>C	XP_016869282.1:p.Ser2236Arg
XM_017013794.1:c.6772A>C	XP_016869283.1:p.Ser2258Arg
XM_017013795.1:c.6601A>C	XP_016869284.1:p.Ser2201Arg
XM_017013796.1:c.6553A>C	XP_016869285.1:p.Ser2185Arg
XM_017013797.1:c.6511A>C	XP_016869286.1:p.Ser2171Arg
XM_017013798.1:c.6772A>C	XP_016869287.1:p.Ser2258Arg
NM_003235.5:c.6772A>C MANE Select	NP_003226.4:p.Ser2258Arg