Canonical Allele Identifier: CA403988324

Gene: TYK2

Linked Data

• dbSNP Id: rs2040960820
• MyVariant Identifiers: chr19:g.10464807T>C (hg19) ; chr19:g.10354131T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354131T>C , CM000681.2:g.10354131T>C	GRCh38
NC_000019.9:g.10464807T>C , CM000681.1:g.10464807T>C	GRCh37
NC_000019.8:g.10325807T>C	NCBI36
NG_007872.1:g.31442A>G , LRG_121:g.31442A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1168A>G	ENSP00000514307.1:n.*1168A>G
ENST00000525976.6:c.2819A>G	ENSP00000434831.2:p.His940Arg
ENST00000527481.3:c.2819A>G	ENSP00000466340.2:p.His940Arg
ENST00000529370.6:n.4195A>G
ENST00000529739.2:n.3233A>G
ENST00000530829.2:c.*2370A>G	ENSP00000436826.2:n.*2370A>G
ENST00000531836.6:c.2819A>G	ENSP00000436175.2:p.His940Arg
ENST00000533334.2:c.*861A>G	ENSP00000432320.2:n.*861A>G
ENST00000534228.2:n.4278A>G
ENST00000699354.1:n.921A>G
ENST00000699355.1:c.*1924A>G	ENSP00000514328.1:n.*1924A>G
ENST00000699356.1:n.3233A>G
ENST00000699357.1:n.4278A>G
ENST00000699358.1:c.2819A>G	ENSP00000514329.1:p.His940Arg
ENST00000699359.1:c.25A>G
ENST00000699360.1:c.2819A>G	ENSP00000514331.1:p.His940Arg
ENST00000699368.1:c.23A>G	ENSP00000514335.1:p.His8Arg
ENST00000525621.6:c.2819A>G MANE Select	ENSP00000431885.1:p.His940Arg
ENST00000264818.10:c.2819A>G	ENSP00000264818.6:p.His940Arg
ENST00000524462.5:c.2264A>G	ENSP00000433203.1:p.His755Arg
ENST00000525621.5:c.2819A>G	ENSP00000431885.1:p.His940Arg
ENST00000527481.2:c.115A>G
ENST00000529412.1:n.491A>G
ENST00000530560.5:c.248A>G	ENSP00000465291.1:p.His83Arg
NM_003331.4:c.2819A>G , LRG_121t1:c.2819A>G	NP_003322.3:p.His940Arg
XM_011528245.1:c.2819A>G	XP_011526547.1:p.His940Arg
XM_011528246.1:c.2522A>G	XP_011526548.1:p.His841Arg
XM_011528247.1:c.2522A>G	XP_011526549.1:p.His841Arg
XM_011528248.1:c.2819A>G	XP_011526550.1:p.His940Arg
XM_011528249.1:c.1493A>G	XP_011526551.1:p.His498Arg
XM_011528251.1:c.1076A>G	XP_011526553.1:p.His359Arg
XM_011528246.3:c.2522A>G	XP_011526548.1:p.His841Arg
XM_011528249.2:c.1493A>G	XP_011526551.1:p.His498Arg
XR_001753750.1:n.2976A>G
XR_001753751.1:n.2976A>G
XR_002958353.1:n.3902A>G
NM_003331.5:c.2819A>G MANE Select	NP_003322.3:p.His940Arg
NM_001385197.1:c.2819A>G	NP_001372126.1:p.His940Arg
NM_001385198.1:c.2819A>G	NP_001372127.1:p.His940Arg
NM_001385199.1:c.2633A>G	NP_001372128.1:p.His878Arg
NM_001385200.1:c.2816A>G	NP_001372129.1:p.His939Arg
NM_001385201.1:c.2621A>G	NP_001372130.1:p.His874Arg
NM_001385202.1:c.2735A>G	NP_001372131.1:p.His912Arg
NM_001385203.1:c.2900A>G	NP_001372132.1:p.His967Arg
NM_001385204.1:c.3029A>G	NP_001372133.1:p.His1010Arg
NM_001385205.1:c.2729A>G	NP_001372134.1:p.His910Arg
NM_001385206.1:c.2693A>G	NP_001372135.1:p.His898Arg
NM_001385207.1:c.2801A>G	NP_001372136.1:p.His934Arg