Canonical Allele Identifier: CA186356709

Gene: TG

Linked Data

• dbSNP Id: rs976522290
• MyVariant Identifiers: chr8:g.134145793G>C (hg19) ; chr8:g.133133549G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133549G>C , CM000670.2:g.133133549G>C	GRCh38
NC_000008.10:g.134145793G>C , CM000670.1:g.134145793G>C	GRCh37
NC_000008.9:g.134214975G>C	NCBI36
NG_015832.1:g.271589G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8077G>C MANE Select	ENSP00000220616.4:p.Gly2693Arg
ENST00000220616.8:c.8077G>C	ENSP00000220616.4:p.Gly2693Arg
ENST00000519178.5:c.3443G>C
ENST00000519543.5:c.2476G>C	ENSP00000430430.1:p.Gly826Arg
ENST00000521107.1:c.289G>C	ENSP00000430161.1:p.Gly97Arg
ENST00000522691.1:n.163G>C
ENST00000523756.5:c.4732G>C
NM_003235.4:c.8077G>C	NP_003226.4:p.Gly2693Arg
XM_005251038.3:c.7885G>C	XP_005251095.1:p.Gly2629Arg
XM_006716622.2:c.8014G>C	XP_006716685.1:p.Gly2672Arg
XM_005251038.4:c.7885G>C	XP_005251095.1:p.Gly2629Arg
XM_006716622.3:c.8014G>C	XP_006716685.1:p.Gly2672Arg
XM_017013793.1:c.8011G>C	XP_016869282.1:p.Gly2671Arg
XM_017013794.1:c.7942G>C	XP_016869283.1:p.Gly2648Arg
XM_017013795.1:c.7906G>C	XP_016869284.1:p.Gly2636Arg
XM_017013796.1:c.7858G>C	XP_016869285.1:p.Gly2620Arg
XM_017013797.1:c.7816G>C	XP_016869286.1:p.Gly2606Arg
NM_003235.5:c.8077G>C MANE Select	NP_003226.4:p.Gly2693Arg