Canonical Allele Identifier: CA372233827

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134030203C>A (hg19) ; chr8:g.133017958C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133017958C>A , CM000670.2:g.133017958C>A	GRCh38
NC_000008.10:g.134030203C>A , CM000670.1:g.134030203C>A	GRCh37
NC_000008.9:g.134099385C>A	NCBI36
NG_015832.1:g.155999C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6743C>A MANE Select	ENSP00000220616.4:p.Pro2248His
ENST00000220616.8:c.6743C>A	ENSP00000220616.4:p.Pro2248His
ENST00000518108.1:c.168+92C>A
ENST00000519178.5:c.2109C>A
ENST00000519543.5:c.1142C>A	ENSP00000430430.1:p.Pro381His
ENST00000522523.5:n.804C>A
ENST00000523756.5:c.3398C>A
NM_003235.4:c.6743C>A	NP_003226.4:p.Pro2248His
XM_005251038.3:c.6551C>A	XP_005251095.1:p.Pro2184His
XM_006716622.2:c.6680C>A	XP_006716685.1:p.Pro2227His
XM_005251038.4:c.6551C>A	XP_005251095.1:p.Pro2184His
XM_006716622.3:c.6680C>A	XP_006716685.1:p.Pro2227His
XM_017013793.1:c.6677C>A	XP_016869282.1:p.Pro2226His
XM_017013794.1:c.6743C>A	XP_016869283.1:p.Pro2248His
XM_017013795.1:c.6572C>A	XP_016869284.1:p.Pro2191His
XM_017013796.1:c.6524C>A	XP_016869285.1:p.Pro2175His
XM_017013797.1:c.6482C>A	XP_016869286.1:p.Pro2161His
XM_017013798.1:c.6743C>A	XP_016869287.1:p.Pro2248His
NM_003235.5:c.6743C>A MANE Select	NP_003226.4:p.Pro2248His