Canonical Allele Identifier: CA463017279

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145885G>C (hg19)

Genomic Alleles

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

Transcript Alleles

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