Canonical Allele Identifier: CA505374060

Gene: TYK2

Linked Data

• dbSNP Id: rs2040963450
• MyVariant Identifiers: chr19:g.10464857A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354181A>T , CM000681.2:g.10354181A>T	GRCh38
NC_000019.9:g.10464857A>T , CM000681.1:g.10464857A>T	GRCh37
NC_000019.8:g.10325857A>T	NCBI36
NG_007872.1:g.31392T>A , LRG_121:g.31392T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1118T>A	ENSP00000514307.1:n.*1118T>A
ENST00000525976.6:c.2769T>A	ENSP00000434831.2:p.Thr923=
ENST00000527481.3:c.2769T>A	ENSP00000466340.2:p.Thr923=
ENST00000529370.6:n.4145T>A
ENST00000529739.2:n.3183T>A
ENST00000530829.2:c.*2320T>A	ENSP00000436826.2:n.*2320T>A
ENST00000531836.6:c.2769T>A	ENSP00000436175.2:p.Thr923=
ENST00000533334.2:c.*811T>A	ENSP00000432320.2:n.*811T>A
ENST00000534228.2:n.4228T>A
ENST00000699354.1:n.871T>A
ENST00000699355.1:c.*1874T>A	ENSP00000514328.1:n.*1874T>A
ENST00000699356.1:n.3183T>A
ENST00000699357.1:n.4228T>A
ENST00000699358.1:c.2769T>A	ENSP00000514329.1:p.Thr923=
ENST00000699360.1:c.2769T>A	ENSP00000514331.1:p.Thr923=
ENST00000525621.6:c.2769T>A MANE Select	ENSP00000431885.1:p.Thr923=
ENST00000264818.10:c.2769T>A	ENSP00000264818.6:p.Thr923=
ENST00000524462.5:c.2214T>A	ENSP00000433203.1:p.Thr738=
ENST00000525621.5:c.2769T>A	ENSP00000431885.1:p.Thr923=
ENST00000527481.2:c.65T>A
ENST00000529412.1:n.441T>A
ENST00000530560.5:c.198T>A	ENSP00000465291.1:p.Thr66=
NM_003331.4:c.2769T>A , LRG_121t1:c.2769T>A	NP_003322.3:p.Thr923=
XM_011528245.1:c.2769T>A	XP_011526547.1:p.Thr923=
XM_011528246.1:c.2472T>A	XP_011526548.1:p.Thr824=
XM_011528247.1:c.2472T>A	XP_011526549.1:p.Thr824=
XM_011528248.1:c.2769T>A	XP_011526550.1:p.Thr923=
XM_011528249.1:c.1443T>A	XP_011526551.1:p.Thr481=
XM_011528251.1:c.1026T>A	XP_011526553.1:p.Thr342=
XM_011528246.3:c.2472T>A	XP_011526548.1:p.Thr824=
XM_011528249.2:c.1443T>A	XP_011526551.1:p.Thr481=
XR_001753750.1:n.2926T>A
XR_001753751.1:n.2926T>A
XR_002958353.1:n.3852T>A
NM_003331.5:c.2769T>A MANE Select	NP_003322.3:p.Thr923=
NM_001385197.1:c.2769T>A	NP_001372126.1:p.Thr923=
NM_001385198.1:c.2769T>A	NP_001372127.1:p.Thr923=
NM_001385199.1:c.2583T>A	NP_001372128.1:p.Thr861=
NM_001385200.1:c.2766T>A	NP_001372129.1:p.Thr922=
NM_001385201.1:c.2571T>A	NP_001372130.1:p.Thr857=
NM_001385202.1:c.2685T>A	NP_001372131.1:p.Thr895=
NM_001385203.1:c.2850T>A	NP_001372132.1:p.Thr950=
NM_001385204.1:c.2979T>A	NP_001372133.1:p.Thr993=
NM_001385205.1:c.2679T>A	NP_001372134.1:p.Thr893=
NM_001385206.1:c.2643T>A	NP_001372135.1:p.Thr881=
NM_001385207.1:c.2751T>A	NP_001372136.1:p.Thr917=