Canonical Allele Identifier: CA463017280

Gene: TG

Linked Data

• dbSNP Id: rs111563366
• MyVariant Identifiers: chr8:g.134145885G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133641G>T , CM000670.2:g.133133641G>T	GRCh38
NC_000008.10:g.134145885G>T , CM000670.1:g.134145885G>T	GRCh37
NC_000008.9:g.134215067G>T	NCBI36
NG_015832.1:g.271681G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8169G>T MANE Select	ENSP00000220616.4:p.Ser2723=
ENST00000220616.8:c.8169G>T	ENSP00000220616.4:p.Ser2723=
ENST00000519178.5:c.3535G>T
ENST00000519543.5:c.2568G>T	ENSP00000430430.1:p.Ser856=
ENST00000521107.1:c.381G>T	ENSP00000430161.1:p.Ser127=
ENST00000522691.1:n.255G>T
ENST00000523756.5:c.4824G>T
NM_003235.4:c.8169G>T	NP_003226.4:p.Ser2723=
XM_005251038.3:c.7977G>T	XP_005251095.1:p.Ser2659=
XM_006716622.2:c.8106G>T	XP_006716685.1:p.Ser2702=
XM_005251038.4:c.7977G>T	XP_005251095.1:p.Ser2659=
XM_006716622.3:c.8106G>T	XP_006716685.1:p.Ser2702=
XM_017013793.1:c.8103G>T	XP_016869282.1:p.Ser2701=
XM_017013794.1:c.8034G>T	XP_016869283.1:p.Ser2678=
XM_017013795.1:c.7998G>T	XP_016869284.1:p.Ser2666=
XM_017013796.1:c.7950G>T	XP_016869285.1:p.Ser2650=
XM_017013797.1:c.7908G>T	XP_016869286.1:p.Ser2636=
NM_003235.5:c.8169G>T MANE Select	NP_003226.4:p.Ser2723=