Canonical Allele Identifier: CA372233898

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134030226G>C (hg19) ; chr8:g.133017981G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133017981G>C , CM000670.2:g.133017981G>C	GRCh38
NC_000008.10:g.134030226G>C , CM000670.1:g.134030226G>C	GRCh37
NC_000008.9:g.134099408G>C	NCBI36
NG_015832.1:g.156022G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6766G>C MANE Select	ENSP00000220616.4:p.Asp2256His
ENST00000220616.8:c.6766G>C	ENSP00000220616.4:p.Asp2256His
ENST00000518108.1:c.168+115G>C
ENST00000519178.5:c.2132G>C
ENST00000519543.5:c.1165G>C	ENSP00000430430.1:p.Asp389His
ENST00000523756.5:c.3421G>C
NM_003235.4:c.6766G>C	NP_003226.4:p.Asp2256His
XM_005251038.3:c.6574G>C	XP_005251095.1:p.Asp2192His
XM_006716622.2:c.6703G>C	XP_006716685.1:p.Asp2235His
XM_005251038.4:c.6574G>C	XP_005251095.1:p.Asp2192His
XM_006716622.3:c.6703G>C	XP_006716685.1:p.Asp2235His
XM_017013793.1:c.6700G>C	XP_016869282.1:p.Asp2234His
XM_017013794.1:c.6766G>C	XP_016869283.1:p.Asp2256His
XM_017013795.1:c.6595G>C	XP_016869284.1:p.Asp2199His
XM_017013796.1:c.6547G>C	XP_016869285.1:p.Asp2183His
XM_017013797.1:c.6505G>C	XP_016869286.1:p.Asp2169His
XM_017013798.1:c.6766G>C	XP_016869287.1:p.Asp2256His
NM_003235.5:c.6766G>C MANE Select	NP_003226.4:p.Asp2256His