Canonical Allele Identifier: CA372231405

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.133975283G>C (hg19) ; chr8:g.132963038G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132963038G>C , CM000670.2:g.132963038G>C	GRCh38
NC_000008.10:g.133975283G>C , CM000670.1:g.133975283G>C	GRCh37
NC_000008.9:g.134044465G>C	NCBI36
NG_015832.1:g.101079G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000220616.9:c.5512G>C MANE Select	ENSP00000220616.4:p.Asp1838His
ENST00000220616.8:c.5512G>C	ENSP00000220616.4:p.Asp1838His
ENST00000518058.1:c.45G>C
ENST00000519178.5:c.878G>C
ENST00000523756.5:c.2167G>C
NM_003235.4:c.5512G>C	NP_003226.4:p.Asp1838His
XM_005251038.3:c.5320G>C	XP_005251095.1:p.Asp1774His
XM_005251040.3:c.5512G>C	XP_005251097.1:p.Asp1838His
XM_005251042.3:c.5512G>C	XP_005251099.1:p.Asp1838His
XM_005251043.3:c.5512G>C	XP_005251100.1:p.Asp1838His
XM_006716622.2:c.5512G>C	XP_006716685.1:p.Asp1838His
XM_005251038.4:c.5320G>C	XP_005251095.1:p.Asp1774His
XM_005251040.4:c.5512G>C	XP_005251097.1:p.Asp1838His
XM_005251042.4:c.5512G>C	XP_005251099.1:p.Asp1838His
XM_006716622.3:c.5512G>C	XP_006716685.1:p.Asp1838His
XM_017013793.1:c.5446G>C	XP_016869282.1:p.Asp1816His
XM_017013794.1:c.5512G>C	XP_016869283.1:p.Asp1838His
XM_017013795.1:c.5341G>C	XP_016869284.1:p.Asp1781His
XM_017013796.1:c.5293G>C	XP_016869285.1:p.Asp1765His
XM_017013797.1:c.5251G>C	XP_016869286.1:p.Asp1751His
XM_017013798.1:c.5512G>C	XP_016869287.1:p.Asp1838His
XM_017013799.1:c.5512G>C	XP_016869288.1:p.Asp1838His
XM_017013800.1:c.5512G>C	XP_016869289.1:p.Asp1838His
NM_003235.5:c.5512G>C MANE Select	NP_003226.4:p.Asp1838His