Canonical Allele Identifier: CA403983215

Gene: TYK2

Linked Data

• dbSNP Id: rs748066182
• gnomAD v2: 19-10463166-C-T
• gnomAD v4: 19-10352490-C-T
• MyVariant Identifiers: chr19:g.10463166C>T (hg19) ; chr19:g.10352490C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352490C>T , CM000681.2:g.10352490C>T	GRCh38
NC_000019.9:g.10463166C>T , CM000681.1:g.10463166C>T	GRCh37
NC_000019.8:g.10324166C>T	NCBI36
NG_007872.1:g.33083G>A , LRG_121:g.33083G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1611G>A	ENSP00000514307.1:n.*1611G>A
ENST00000525976.6:c.3262G>A	ENSP00000434831.2:p.Gly1088Arg
ENST00000527481.3:c.*32G>A	ENSP00000466340.2:n.*32G>A
ENST00000529370.6:n.4638G>A
ENST00000529739.2:n.4071G>A
ENST00000530829.2:c.*2813G>A	ENSP00000436826.2:n.*2813G>A
ENST00000531836.6:c.3262G>A	ENSP00000436175.2:p.Gly1088Arg
ENST00000533334.2:c.*1242+436G>A	ENSP00000432320.2:n.*1242+436G>A
ENST00000534228.2:n.5054+436G>A
ENST00000699354.1:n.1364G>A
ENST00000699355.1:c.*2762G>A	ENSP00000514328.1:n.*2762G>A
ENST00000699356.1:n.4071G>A
ENST00000699357.1:n.5116G>A
ENST00000699358.1:c.3200+436G>A	ENSP00000514329.1:n.3200+436G>A
ENST00000699359.1:c.436G>A
ENST00000699360.1:c.3220G>A	ENSP00000514331.1:p.Gly1074Arg
ENST00000699361.1:n.296G>A
ENST00000699362.1:c.158G>A	ENSP00000514332.1:n.158G>A
ENST00000699363.1:c.158G>A	ENSP00000514333.1:n.158G>A
ENST00000699364.1:n.262G>A
ENST00000699365.1:c.331G>A	ENSP00000514334.1:p.Gly111Arg
ENST00000699366.1:n.111+1324G>A
ENST00000699367.1:n.111+1324G>A
ENST00000699368.1:c.749G>A	ENSP00000514335.1:n.749G>A
ENST00000525621.6:c.3262G>A MANE Select	ENSP00000431885.1:p.Gly1088Arg
ENST00000264818.10:c.3262G>A	ENSP00000264818.6:p.Gly1088Arg
ENST00000524462.5:c.2707G>A	ENSP00000433203.1:p.Gly903Arg
ENST00000525621.5:c.3262G>A	ENSP00000431885.1:p.Gly1088Arg
ENST00000525976.5:c.3G>A
ENST00000527481.2:c.439G>A
ENST00000529422.1:n.116+532G>A
ENST00000529739.1:c.331G>A	ENSP00000436155.1:p.Gly111Arg
ENST00000530220.1:n.331+436G>A
ENST00000530560.5:c.338-1522G>A	ENSP00000465291.1:n.338-1522G>A
ENST00000592137.1:n.416G>A
NM_003331.4:c.3262G>A , LRG_121t1:c.3262G>A	NP_003322.3:p.Gly1088Arg
XM_011528245.1:c.3262G>A	XP_011526547.1:p.Gly1088Arg
XM_011528246.1:c.2965G>A	XP_011526548.1:p.Gly989Arg
XM_011528247.1:c.2965G>A	XP_011526549.1:p.Gly989Arg
XM_011528248.1:c.3200+436G>A	XP_011526550.1:n.3200+436G>A
XM_011528249.1:c.1936G>A	XP_011526551.1:p.Gly646Arg
XM_011528251.1:c.1519G>A	XP_011526553.1:p.Gly507Arg
XM_011528246.3:c.2965G>A	XP_011526548.1:p.Gly989Arg
XM_011528249.2:c.1936G>A	XP_011526551.1:p.Gly646Arg
XR_001753750.1:n.3357+436G>A
XR_001753751.1:n.3814G>A
XR_002958353.1:n.4740G>A
NM_003331.5:c.3262G>A MANE Select	NP_003322.3:p.Gly1088Arg
NM_001385197.1:c.3262G>A	NP_001372126.1:p.Gly1088Arg
NM_001385198.1:c.3168+468G>A	NP_001372127.1:n.3168+468G>A
NM_001385199.1:c.3076G>A	NP_001372128.1:p.Gly1026Arg
NM_001385200.1:c.3259G>A	NP_001372129.1:p.Gly1087Arg
NM_001385201.1:c.3064G>A	NP_001372130.1:p.Gly1022Arg
NM_001385202.1:c.3178G>A	NP_001372131.1:p.Gly1060Arg
NM_001385203.1:c.3343G>A	NP_001372132.1:p.Gly1115Arg
NM_001385204.1:c.3472G>A	NP_001372133.1:p.Gly1158Arg
NM_001385205.1:c.3172G>A	NP_001372134.1:p.Gly1058Arg
NM_001385206.1:c.3136G>A	NP_001372135.1:p.Gly1046Arg
NM_001385207.1:c.3244G>A	NP_001372136.1:p.Gly1082Arg