Canonical Allele Identifier: CA463017221

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145846G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133602G>C , CM000670.2:g.133133602G>C	GRCh38
NC_000008.10:g.134145846G>C , CM000670.1:g.134145846G>C	GRCh37
NC_000008.9:g.134215028G>C	NCBI36
NG_015832.1:g.271642G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8130G>C MANE Select	ENSP00000220616.4:p.Leu2710=
ENST00000220616.8:c.8130G>C	ENSP00000220616.4:p.Leu2710=
ENST00000519178.5:c.3496G>C
ENST00000519543.5:c.2529G>C	ENSP00000430430.1:p.Leu843=
ENST00000521107.1:c.342G>C	ENSP00000430161.1:p.Leu114=
ENST00000522691.1:n.216G>C
ENST00000523756.5:c.4785G>C
NM_003235.4:c.8130G>C	NP_003226.4:p.Leu2710=
XM_005251038.3:c.7938G>C	XP_005251095.1:p.Leu2646=
XM_006716622.2:c.8067G>C	XP_006716685.1:p.Leu2689=
XM_005251038.4:c.7938G>C	XP_005251095.1:p.Leu2646=
XM_006716622.3:c.8067G>C	XP_006716685.1:p.Leu2689=
XM_017013793.1:c.8064G>C	XP_016869282.1:p.Leu2688=
XM_017013794.1:c.7995G>C	XP_016869283.1:p.Leu2665=
XM_017013795.1:c.7959G>C	XP_016869284.1:p.Leu2653=
XM_017013796.1:c.7911G>C	XP_016869285.1:p.Leu2637=
XM_017013797.1:c.7869G>C	XP_016869286.1:p.Leu2623=
NM_003235.5:c.8130G>C MANE Select	NP_003226.4:p.Leu2710=