Canonical Allele Identifier: CA372233924

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134030236A>C (hg19) ; chr8:g.133017991A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133017991A>C , CM000670.2:g.133017991A>C	GRCh38
NC_000008.10:g.134030236A>C , CM000670.1:g.134030236A>C	GRCh37
NC_000008.9:g.134099418A>C	NCBI36
NG_015832.1:g.156032A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6776A>C MANE Select	ENSP00000220616.4:p.Lys2259Thr
ENST00000220616.8:c.6776A>C	ENSP00000220616.4:p.Lys2259Thr
ENST00000518108.1:c.168+125A>C
ENST00000519178.5:c.2142A>C
ENST00000519543.5:c.1175A>C	ENSP00000430430.1:p.Lys392Thr
ENST00000523756.5:c.3431A>C
NM_003235.4:c.6776A>C	NP_003226.4:p.Lys2259Thr
XM_005251038.3:c.6584A>C	XP_005251095.1:p.Lys2195Thr
XM_006716622.2:c.6713A>C	XP_006716685.1:p.Lys2238Thr
XM_005251038.4:c.6584A>C	XP_005251095.1:p.Lys2195Thr
XM_006716622.3:c.6713A>C	XP_006716685.1:p.Lys2238Thr
XM_017013793.1:c.6710A>C	XP_016869282.1:p.Lys2237Thr
XM_017013794.1:c.6776A>C	XP_016869283.1:p.Lys2259Thr
XM_017013795.1:c.6605A>C	XP_016869284.1:p.Lys2202Thr
XM_017013796.1:c.6557A>C	XP_016869285.1:p.Lys2186Thr
XM_017013797.1:c.6515A>C	XP_016869286.1:p.Lys2172Thr
XM_017013798.1:c.6776A>C	XP_016869287.1:p.Lys2259Thr
NM_003235.5:c.6776A>C MANE Select	NP_003226.4:p.Lys2259Thr