Canonical Allele Identifier: CA372233772

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134030193G>T (hg19) ; chr8:g.133017948G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133017948G>T , CM000670.2:g.133017948G>T	GRCh38
NC_000008.10:g.134030193G>T , CM000670.1:g.134030193G>T	GRCh37
NC_000008.9:g.134099375G>T	NCBI36
NG_015832.1:g.155989G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6733G>T MANE Select	ENSP00000220616.4:p.Ala2245Ser
ENST00000220616.8:c.6733G>T	ENSP00000220616.4:p.Ala2245Ser
ENST00000518108.1:c.168+82G>T
ENST00000519178.5:c.2099G>T
ENST00000519543.5:c.1132G>T	ENSP00000430430.1:p.Ala378Ser
ENST00000522523.5:n.794G>T
ENST00000523756.5:c.3388G>T
NM_003235.4:c.6733G>T	NP_003226.4:p.Ala2245Ser
XM_005251038.3:c.6541G>T	XP_005251095.1:p.Ala2181Ser
XM_006716622.2:c.6670G>T	XP_006716685.1:p.Ala2224Ser
XM_005251038.4:c.6541G>T	XP_005251095.1:p.Ala2181Ser
XM_006716622.3:c.6670G>T	XP_006716685.1:p.Ala2224Ser
XM_017013793.1:c.6667G>T	XP_016869282.1:p.Ala2223Ser
XM_017013794.1:c.6733G>T	XP_016869283.1:p.Ala2245Ser
XM_017013795.1:c.6562G>T	XP_016869284.1:p.Ala2188Ser
XM_017013796.1:c.6514G>T	XP_016869285.1:p.Ala2172Ser
XM_017013797.1:c.6472G>T	XP_016869286.1:p.Ala2158Ser
XM_017013798.1:c.6733G>T	XP_016869287.1:p.Ala2245Ser
NM_003235.5:c.6733G>T MANE Select	NP_003226.4:p.Ala2245Ser